Aryloxy- and arylthio-fused pyridines and pyrimidines and derivatives

Corticotropin releasing factor (herein referred to as CRF), a 41 amino acid peptide, is the primary physiological regulator of proopiomelanocortin(POMC) -derived peptide secretion from the anterior pituitary gland [J. Rivier et al., Proc. Nat. Acad. Sci. (USA) 80:4851 (1983); W. Vale et al., Science 213:1394 (1981)]. In addition to its endocrine role at the pituitary gland, immunohistochemical localization of CRF has demonstrated that the hormone has a broad extrahypothalamic distribution in the central nervous system and produces a wide spectrum of autonomic, electrophysiological and behavioral effects consistent with a neurotransmitter or neuromodulator role in brain [W. Vale et al., Rec. Prog. Horm. Res. 39:245 (1983); G.F. Koob, Persp. Behav. Med. 2:39 (1985); E.B. De Souza et al., J. Neurosci. 5:3189 (1985)] . There is also evidence that CRF plays a significant role in integrating the response of the immune system to physiological, psychological, and immunological stressors [J.E. Blalock, Physiological Reviews 69:1 (1989); J.E. Clinical data provide evidence that CRF has a role in psychiatric disorders and neurological diseases including depression, anxiety-related disorders and feeding disorders. A role for CRF has also been postulated in the etiology and pathophysiology of Alzheimer's disease, Parkinson's disease, Huntington's disease, progressive supranuclear palsy and amyotrophic lateral sclerosis as they relate to the dysfunction of CRF neurons in the central nervous system [for review see E.B. De Souza, Hosp. Practice 23:59 (1988)]. In affective disorder, or major depression, the concentration of CRF is significantly increased in the cerebral spinal fluid (CSF) of drug-free individuals [C.B. Nemeroff et al., Science 226:1342 (1984); C.M. Banki et al., Am. J. Psychiatry 144:873 (1987); R.D. France et al., Biol. Psychiatry 28:86 (1988); M. Arato et al., Biol Psychiatry 25:355 (1989)]. Furthermore, the density of CRF receptors is significantly decreased in the frontal cortex of suicide victims, consistent with a hypersecretion of CRF [C.B. Nemeroff et al., Arch. Gen. Psychiatry 45:577 (1988)]. In addition, there is a blunted adrenocorticotropin (ACTH) response to CRF (i.v. administered) observed in depressed patients [P.W. Gold et al., Am J. Psychiatry 141:619 (1984); F. Holsboer et al., Psychoneuroendocrinology 9:147 (1984); P.W. Gold et al., New Eng. J. Med. 314:1129 (1986)]. Preclinical studies in rats and non-human primates provide additional support for the hypothesis that hypersecretion of CRF may be involved in the symptoms seen in human depression [R.M. Sapolsky, Arch. Gen. Psychiatry 46:1047 (1989)]. There is preliminary evidence that tricyclic antidepressants can alter CRF levels and thus modulate the numbers of CRF receptors in brain [Grigoriadis et al., Neuropsychopharmacology2:53 (1989)]. There has also been a role postulated for CRF in the etiology of anxiety-related disorders. CRF produces anxiogenic effects in animals and interactions between benzodiazepine / nonbenzodiazepine anxiolytics and CRF have been demonstrated in a variety of behavioral anxiety models [D.R. Britton et al., Life Sci. 31:363 (1982); C.W. Berridge and A.J. Dunn Regul. Peptides 16:83 (1986)]. Preliminary studies using the putative CRF receptor antagonist a-helical ovine CRF (9-41) in a variety of behavioral paradigms demonstrate that the antagonist produces "anxiolytic-like" effects that are qualitatively similar to the benzodiazepines [C.W. Berridge and A.J. Dunn Horm. Behav. 21:393 (1987), Brain Research Reviews 15:71 (1990)]. Neurochemical, endocrine and receptor binding studies have all demonstrated interactions between CRF and benzodiazepine anxiolytics providing further evidence for the involvement of CRF in these disorders. Chlordiazepoxide attenuates the "anxiogenic" effects of CRF in both the conflict test [K.T. Britton et al., Psychopharmacology 86:170 (1985); K.T. Britton et al., Psychopharmacology 94:306 (1988)] and in the acoustic startle test [N.R. Swerdlow et al., Psychopharmacology 88:147 (1986)] in rats. The benzodiazepine receptor antagonist (Ro15-1788), which was without behavioral activity alone in the operant conflict test, reversed the effects of CRF in a dosedependent manner while the benzodiazepine inverse agonist (FG7142) enhanced the actions of CRF [K.T. Britton et al., Psychopharmacology 94:306 (1988)]. The mechanisms and sites of action through which the standard anxiolytics and antidepressants produce their therapeutic effects remain to be elucidated. It has been hypothesized however, that they are involved in the suppression of the CRF hypersecretion that is observed-in these disorders. Of particular interest is that preliminary studies examining the effects of a CRF receptor antagonist (a - helical CRF9-41) in a variety of behavioral paradigms have demonstrated that the CRF antagonist produces "anxiolytic-like" effects qualitatively similar to the benzodiazepines [for review see G.F. Koob and K.T. Britton, In: Corticotropin-Releasing Factor: Basic and Clinical Studies of a Neuropeptide, E.B. De Souza and C.B. Nemeroff eds., CRC Press p221 (1990)]. DuPont Merck PCT application US94/II050 describes corticotropin releasing factor antagonist compounds of the formula: R 3 RI V N /R4 I K M L and their use to treat psychiatric disorders and neurological diseases. Included in the description are fused pyridines and pyrimidines of the formula: where: Z is CR 2 or N; A is CR 30 or N; D is CR 28 or N; and R 3 can be aryloxy or arylthio. Pfizer WO 95/33750 describes corticotropin releasing factor antagonist compounds useful in the treatment of CNS and stress disorders. The description includes compounds of the formulae: where A is CR7 or N; B is OCHRIR2 or SCHRIR2; R1 is substituted or unsubstituted alkyl; R2 is substituted or unsubstituted alkyl, aryl or heteroaryl; R3 is methyl, halo, cyano, methoxy, etc.; R4 is H, substituted or unsubstituted alkyl, halo, amino, nitro, etc. ; R5 is substituted or unsubstituted aryl or heteroaryl; R6 is H or substituted or unsubstituted alkyl; R7 is H, methyl, halo, cyano, etc. ; RI6 and RI7 taken together form an oxo (=0) group; and G is =0, =S, =NH, =NCH3, hydrogen, methyl, methoxy, etc. Pfizer WO 95/34563 describes corticotropin releasing factor antagonist compounds, including compounds of the formula: R 3 R, N m m R 3/ i -I Rs R 4 where A, B and the R groups have definitions similar those in WO 95/33750. Pfizer WO 95/33727 describes corticotropin releasing factor antagonist compounds of the formula: RI N/N I Y where A is CH2 and Z can be a heteroaryl moiety. Ganguly et al., U.S. Patent 4,076,711 describes triazolo[4,5-d]pyrimidines of the formula: where X is halo, -NRIR or alkoxy, with R1 and R each being H or alkyl;- Y is alkyl, cycloalkyl, hydroxycycloalkyl, phenyl, bicycloalkyl or phenylalkyl or bicycloalkylalkyl; and Q is H or Y. The patent states that the compounds are useful in the treatment psoriasis. Tanji et al., Chem. Pharm. Bull. 39(11)30373040 (1991), describes triazolo[4,5-d]pyrimidines of the formula: II , 2N .,,1 4 .... 3 / Ph Ph Ph Me N N where halo is I, Br or CI, Ph is phenyl and Me is methyl. No utility for the compounds is described. Settimo et al., II Farmaco, Ed. Sc., 35 (4), 308-323 (1980) describes 8-azaadenines (triazolo[4,5-d] pyrimidines) of the formula: L %N N N !, H N N where R1 is H or benzyl and R2 is p-methylphenyl. Biagi et al., I1 Farmaco, 49 (3), 183-186 (1994), describes N(6)-substituted 2-n-butyl-9-benzyl-8azaadenines of the formula: CH 2 CsHs H N N where R 2 can be alkyl, phenyl, or benzyl. The paper states that the compounds have affinity for adenosine receptors. Thompson et al., J. Med. Chem., 1991, 34, 28772882, describes N6,9-disubstituted adenines of the formula: Phenyl H or CI Ph N N CH 3 I H or I H CH 3 where Ph is phenyl or (when C-2 is unsubstituted) 2fluorophenyl. The paper states that the compounds have selective affinity for the A1 adenosine receptor. Kelley et al., J. Med. Chem. 1990, 31, 606-612, describes the compound where R 6 is NHC 6 H5 and R 9 is CH2C6H5, and reports that the compound was inactive when tested for anticonvulsant activity. The paper reports that various 6- (alkylamino)-9-benzyl-9H-purine analogs of the above compound exhibited anticonvulsant activity. Kelley et al., J. Med. Chem. 1990, 33, 1360-1363, describes 6-anilino-9-benzyl-2-choro-9H-purines of the formula: Cl mR4 R 4 N/ m m ' Bz Cl where Bz is benzyl or (when R 4 is H) p-methylbenzyl and R 4 is H or alkyl, alkoxy, halo, cyano, nitro, etc. Tests of the compounds for antirhinoviral activity are reported. Kelley et al., J. Heterocyclic Chem., 28, 1099 (1991), describes 6-substituted-9-(3-formamidobenzyl)- 9H-purines of the formula: NHCsHs N m CsHsHN "o'R I CH 2 CsH 4-o-R 1 where R1 is NH2 or NHCH0. The compound where R1 is NHCHO was tested for benzodiazepine receptor binding was inactive, although various analogs were active. Khairy et al., J. Heterocyclic Chem., 22, (1985), describes synthesis of certain 9-aryl-9H-purin6-amines of the formula: R 1 R 2 R 3 R 4 R 3 R 2 .,o/22 N CH 3 = NH CH where the R groups are H, methyl, ethyl, isopropyl, chloro or fluoro. Hoechst EP 298467 (1989) describes azapurine derivatives, including compounds of the structure: where Q is O, S, SO, S02 or NH2; X is O, S, SO or S02; Z is H, halogen, CF@, I-3C alkoxy or alkylthio; R 2 is alkyl or alkoxy; R 3 is OR 2These compounds are claimed to be useful for treating virus diseases, autoimmune diseases and cancers. SS Pharmaceutical Co. Jp 59062595 (1984) and Jp 56131587 (1981) describe triazolopyrimidine derivatives, including compounds of the structure: where Q is O, S, S0 2 ; R is amino or substituted amino, alkoxy, benzyloxy, halogen, or phenylhydrazino. These compounds are claimed to be useful as anticancer agents. R N N Fuji Jp 60194443 (1985) describe aza-indenes, including compounds of the structure: R 1 N Q N R N R 3 where Q is O, S; R I, R 2 and R 3 are H, alkyl, aryl, aralkyl, amino, hydroxyl, alkoxy, carbamoyl, aryloxy, alkoxy carbonyl, cyano, halogen, alkylthio, arylthio, carboxyl, or mercapto, provided that at least one of the substituents is mercapto. These compounds are claimed to be useful as light-sensitizing agents, providing high photographic speed and contrast to silver halide emulsions. SUMMARY OF THE INVENTION This invention is a class of novel compounds which are CRF receptor antagonists and which can be represented by formula I or formula II: R 1 R 1 Z Ar Q Z N //N" R13 G I II or a pharmaceutically acceptable salt or pro-drug form thereof, wherein: x is N or CRI; Y is N or CR2; Z is NR 3, O, or S (O)n; G is O or S; Q is O or S(O)n Ar is phenyl, naphthyl, pyridyl, pyrimidinyl, triazinyl, furanyl, quinolinyl, isoquinolinyl, thienyl, imidazolyl, thiazolyl, indolyl, pyrrolyl, oxazolyl, benzofuranyl, benzothienyl, benzthiazolyl, isoxazolyl or pyrazolyl, each optionally substituted with 1 to 4 R 5 groups; independently at each occurrence H, CIC4 alkyl, C2-C4 alkenyl, C2-C4 alkynyl, halo, CN, CI-C4 haloalkyl, -NR9R I0, NR9COR I0, -OR II, SH or -S(O)nRI2; H, CI-C4 alkyl, CI-C6 cycloalkyl, halo, CN, -NR6R 7, NR9COR I0, CI-C4 haloalkyl, -OR 7, SH or -S (O) nR 12 ; H, CI-CI0 alkyl, C2-Ci0 alkenyl, C2Cl0 alkynyl, C3-C8 cycloalkyl or C4C12 cycloalkylalkyl each optionally substituted with 1 to 3 substituents independently selected at each occurrence from CI-C6 alkyl, C3-C6 cycloalkyl, halo, CI-C4 haloalkyl, cyano, -OR 7, SH, -S(O)n RI3, -COR 7, -C02R 7, -OC(O)R 13, -NR8COR 7, -N(COR7) 2 , -NR8CONR6R 7, -NR8CO 2 RI3, -NR6R 7, -CONR6R 7, aryl, heteroaryl and heterocyclyl, where the aryl, heteroaryl or heterocyclyl is optionally substituted with 1 to 3 substituents independently selected at each occurrence from CI-C6 alkyl, C3-C6 cycloalkyl, halo, CI-C4 haloalkyl, cyano, -OR 7, SH, -S(O)n RI3, -COR 7, -C02 R7, -OC(O)R 13, -NR8COR 7, -N(COR7) 2, -NR8CONR6R 7, -NR8CO 2 RI3, -NR6R 7, and -CONR6R7; independently at each occurrence CI-CI0 alkyl, C2-CI0 alkenyl, C2-CI0 alkynyl, C3-C6 cycloalkyl, C4-C12 cycloalkylalkyl, -NO2, halo, -CN, CI-C4 haloalkyl, -NR6R 7, NRsCOR 7, NRSCO 2 R7, -COR 7 -OR 7, -CONR6R 7, -CO(NOR9)R 7, C02R 7, or -S(O)n R7, where CI-CI0 alkyl, C2-CI0 alkenyl, C2-CI0 alkynyl, C3-C6 cycloalkyl and C4C12 cycloalkylalkyl are optionally substituted with 1 to 3 substituents independently selected at each occurrence from CI-C4 alkyl, -NO2, halo, -CN, -NR6R7,--NR6R 7, NRSCOR 7, NRSCO 2 R7, -COR 7 -OR 7, -CONR6R 7, C02 R7, -CO(NOR9)R 7, or -S(O)nR7; and R7 are independently at each occurrence H, CI-C4 alkyl, CI-C4 haloalkyl, C2-C8 alkoxyalkyl, C3-C6 cycloalkyl, C4-C12 cycloalkylalkyl, aryl, aryl (CI-C4 alkyl)-, heteroaryl or heteroaryl (CI-C4 alkyl)-; or NR6R 7 is piperidine, pyrrolidine, piperazine, Nmethylpiperazine, morpholine or thiomorpholine; independently at each occurrence H or CI-C4 alkyl; and R I0 are independently at each occurrence selected from H, CI-C4 alkyl, or C3-C6 cycloalkyl ; is H, CI-C4 alkyl, CI-C4 haloalkyl, .or C3-C6 cycloalkyl; is CI-C4 alkyl or CI-C4 haloalkyl; is CI-C4 alkyl, CI-C4 haloalkyl, C2-C8 alkoxyalkyl, C3-C6 cycloalkyl, C4C12 cycloalkylalkyl, aryl, aryl(Cl-C4 alkyl)-, heteroaryl or heteroaryl (CI-C4 alkyl)-; is phenyl or naphthyl, each optionally substituted with 1 to 3 substituents independently selected at each occurrence from CI-C6 alkyl, C3-C6 cycloalkyl, halo, CIC4 haloalkyl, cyano, -OR 7, SH, -S (O)nR 13, -COR 7, -NR8COR 7, heteroaryl is pyridyl, pyrimidinyl, triazinyl, furanyl, quiaolinyl, isoquinolinyl, thienyl, imidazolyl, thiazolyl, indolyl, pyrrolyl, oxazolyl, benzofuranyl, benzothienyl, benzthiazolyl, isoxazolyl or pyrazolyl optionally substituted with 1 to 3 substituents independently selected at each occurrence from CI-C6 alkyl, C3-C6 cycloalkyl, halo, CIC4 haloalkyl, cyano, -OR 7, SH, -S (O)n RI3, -COR 7, -C02 R7, -OC(O)R 13, -NRSCOR 7, -N(COR 7) 2, -NR8CONR6R7, -NR8CO 2 RI3, -NR6R 7, and -CONR6R 7 ; heterocyclyl is saturated or partially saturated heteroaryl, optionally substituted with 1 to 3 substituents independently selected at each occurrence from CI-C6 alkyl, C3-C6 cycloalkyl, halo, CI-C4 haloalkyl, cyano, -OR 7, SH, -S(O)n RI3, -COR 7, -C02 R7, -OC(O)R 13, -NR8COR 7, -N(COR 7) 2, -NR8CONR6R7, -NR8C0 2 RI3, -NR6R7, and -CONR6R 7; n is independently at each occurrence 0, 1 or 2; provided that in formula I, when X and Z are each N Y is CR 2, then R 1 and R 2 cannot be mercapto groups. Included in this invention is the method of treating affective disorder, anxiety, depression, irritable bowel syndrome, post-traumatic stress disorder, supranuclear palsy, immune suppression, Alzheimer's disease, gastrointestinal disease, anorexia nervosa or other feeding disorder, drug or alcohol withdrawal symptoms, drug addiction, inflammatory disorder, or fertility problem in a mammal comprising administering to the mammal a therapeutically effective amount of a compound of formula I or II. Also included in this invention are o pharmaceutical compositions comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of any one of the above-described compounds. The compounds provided by this invention (and especially labelled compounds of this invention) are also useful as standards and reagents in determining the ability of a potential pharmaceutical to bind to the CRF receptor. DETAILED DESCRIPTION OF INVENTION Many compounds of this invention have one or more asymmetric centers or planes. Unless otherwise indicated, all chiral (enantiomeric and diastereomeric) and racemic forms are included in the present invention. Many geometric isomers of olefins, C=N double bonds, and the like can also be present in the compounds, and all such stable isomers are contemplated in the present invention. The compounds may be isolated in optically active or racemic forms. It is well known in the art how to prepare optically active forms, such as by resolution of racemic forms or by synthesis from optically active starting materials. All chiral, (enantiomeric and diastereomeric) and racemic forms and all geometric isomeric forms of a structure are intended, unless the specific stereochemistry or isomer form is specifically indicated. The term "alkyl" includes both branched and straight-chain alkyl having the specified number of carbon atoms. "Alkenyl" includes hydrocarbon chains of either a straight or branched configuration and one or more unsaturated carbon-carbon bonds which may occur in any stable point along the chain, such as ethenyl, propenyl, and the like. "Alkynyl" includes hydrocarbon chains of either a straight or branched configuration and one or more triple carbon-carbon bonds which may occur in any stable point along the chain, such as ethynyl, propynyl and the like. "Haloalkyl" is intended to include both branched and straight-chain alkyl having the specified number of carbon atoms, substituted with 1 or more halogen; "alkoxy" represents an alkyl group of indicated number of carbon atoms attached through an oxygen bridge; "cycloalkyl" is intended to include saturated ring groups, including mono-,bior poly-cyclic ring systems, such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and so forth. "Halo" or "halogen" includes fluoro, chloro, bromo, and iodo. The term "substituted", as used herein, means that one or more hydrogen on the designated atom is replaced with a selection from the indicated group, provided that the designated atom's normal valency is not exceeded, and that the substitution results in a stable compound. When a substitent is keto (i.e., =O), then 2 hydrogens on the atom are replaced. Combinations of substituents and/or variables are permissible only if such combinations result in stable compounds. By "stable compound" or "stable structure" is meant a compound that is sufficiently robust to survive isolation to a useful degree of purity from a reaction mixture, and formulation into an efficacious therapeutic agent. The term "pharmaceutically acceptable salts" includes acid or base salts of the compounds of formulas (I) and (II). Examples of pharmaceutically acceptable salts include, but are not limited to, mineral or organic acid salts of basic residues such as amines; alkali or organic salts of acidic residues such as carboxylic acids; and the like. Pharmaceutically acceptable salts of the compounds of the-invention can be prepared by reacting the free acid or base forms of these compounds with a stoichiometric amount of the appropriate base or acid in water or in an organic solvent, or in a mixture of the two; generally, nonaqueous media like ether, ethyl acetate, ethanol, isopropanol, or acetonitrile are preferred. Lists of suitable salts are found in Pharmaceutical Sciences, 17th ed., Mack Publishing Company, Easton, PA, 1985, p. 1418, the disclosure of which is hereby incorporated by reference. "Prodrugs" are considered to be any covalently bonded carriers which release the active parent drug of formula (I) or (II) in vivo when such prodrug is administered to a mammalian subject. Prodrugs of the compounds of formula (I) and (II) are prepared by modifying functional groups present in the compounds in such a way that the modifications are cleaved, either in routine manipulation or in vivo, to the parent compounds. Prodrugs include compounds wherein hydroxy, amine, or sulfhydryl groups are bonded to any group that, when administered to a mammalian subject, cleaves to form a free hydroxyl, amino, or sulfhydryl group, respectively. Examples of prodrugs include, but are not limited to, acetate, formate and benzoate derivatives of alcohol and amine functional groups in the compounds of formulas (I) and (II) ; and the like. The term "therapeutically effective amount" of a compound of this invention means an amount effective to antagonize abnormal level of CRF or treat the symptoms of affective disorder, anxiety or depression in a host. Synthesis The novel substituted fused pyrimidines of the present inventionare prepared by one of the general schemes outlined below wherein At, Q, G, X, Y, Z, RI, R2° R3 and R 13 are as above and L represents a suitable leaving group such as halo, methanesulfonate, ptoluenesulfonate, or triflate. Scheme I R 1 ¢N L Ar-QH + N - NO 2 Ar"Q I L III II .R 3 R 1 N, Ar-Q Ar"Q Ar SQ IV v v1 R 3 R 1 Ny%>...R 2 R 1 NyN G Ar.Q R 13 Ar"Q VII VIII Compounds of the type III (Scheme i) are prepared by condensing the alkali metal salts of compounds of the type I, where Q = 0 or S, with compounds of the type II madeaccording to literature procedures [Ashley and Harris, J Chem Soc., 677(1944); Albert et al., J Chem Soc., 3832(1954)] in solvents such as acetonitrile at temperatures between 0 and 50oc. Compounds of the type IV are obtained from compounds of the type III by treatment with primary amines such as 4-aminoheptane in solvents such as dioxane at temperatures between 25 and 100oc. These amino adducts are converted into compounds of the type V by reduction with hydrogen in the presence of catalysts such as platinum on carbon at atmospheric or elevated pressure or by reducing agents such as sodium dithionite, or iron in acetic acid. Compounds of the type VI are prepared from compounds of the type V through diazotization and cyclization with an alkali metal nitrite in the presence of an acid in water with or without an organic cosolvent such as cyclic ethers or aromatic hydrocarbons. Compounds of type VII are prepared by the condensation of compounds of the type V with phosgene, thiophosgene, carbonyldiimidazole, thiocarbonyldiimidazole, urea, thiourea, guanidine and the like, in the presence or absence of solvents such as high-boilng ethers or aromatic hydrocarbons and at temperatures between I00-200°C. Scheme 2 R 3 R 3 RI I N yNH R 1 "'-€'N " N. II "1 N N NH 2 NNHR, 3 N'x b " C1 C1 C1 XI IX X R 1 "-,,.,/N , N, VII II -I / "-R 2 N" N C1 RI VIII C1 R 13 XIII XlI Compounds of the type VIII are prepared by condensation of the compounds of the type V with reagents such as acids, acid chlorides, anhydrides, amides or ortho esters in the presence or absence of solvents such as ethers or aromatic hydrocarbons at temperatures between 0 to 200°C. Compounds of the type VII, where R 13 = H, are alkylated with reagents such as alkyl halides and the like, in the presence or absence of bases such as sodium hydroxide, in solvents such as tetrahydrofuran or DMF and at temperatures between 0 to 100°C to yield compounds of the type VIII. Alternatively, compounds of the type VII are prepared from compounds of the type X (Scheme 2). These diamino pyrimidines, X, are made from the dichloroaminopyrimidines of type IX which are synthesized from compounds of type II by treatment with reducing agents such as, but not limited to sodium dithionite, iron or zinc in the presence of acid, or catalytic hydrogenation (see: LaRock, Comprehensive Organic Transformations, VCH Publishers, NY, 1989, 411). The diamino compounds, X, are converted into compounds of the type XII using the same procedure as_described for the preparation of compounds of the type VII from compounds of the type V, and then condensing compounds of the type XII with salts of the compounds of the type I in solvents such as DMF or 2-ethoxyethanol at temperatures between 25 and 200 0C. Alternatively, compounds of the type VIII are prepared from compounds of the type X by first converting them into compounds of the type XIII using the same method as described for the preparation of compounds of the type VIII from compounds of the type V and then condensing compounds of the type XIII thus obtained with salts of the compounds of the type I under the conditions described for the conversion of compounds of the type I into compounds of the type II. Alternatively, compounds of type VI are prepared from compounds of type X by diazotization and cyclization, as previously described for compounds of compound type V to compounds of type VI, to give compounds of type XI. Subsequent treatment with the salts of the compounds of the type I with compounds of type XI, as previously described, provides these tiazolo adducts of type VI. The compounds of the present invention and their synthesis are further illustrated by the following examples and preparations. 3-Bromo-4-hvdroxv-5-methoxvacetonhenone Bromine (9.62g) in 30mL of chloroform was added dropwise to a solution of acetovanillone (10.0g) in 150mL of chloroform maintained at 0-5 °C, such that the temperature did not rise above 5 °C. After the addition was complete, the mixture was stirred at 0-5°C for 4 hours. The residue was treated with water. The organic layer was dried aver MgSO 4 and stripped of the solvent under reduced pressure to yield a pinkish powder which was tritrated with ether and filtered to yield the title compopund, mp 148-152 °C. 3-Bromo-4-hvdroxv-5-methoxv- -dimethvlbenzenemethanol Methyl magnesium bromide (3M in diethyl ether, ll.42mL) was added dropwise to a solution of 5-Bromo-4-hydroxy3-methoxyacetophenone (3.0g) in anhydrous tetrahydrofuran (60mL) maintained at 0-5 °C under N 2 gas, such that the temperature did not rise above 5 °C. After the addition was complete, the solution was stirred at room temperature for 2 hours. Saturated ammonium chloride was added dropwise until effervescence ceased. The mixture was treated with an excess of saturated ammonium chloride. The organic layer was dried over MgS0 4 and stripped of the solvent under reduced pressure to yield the title compound as a viscous oil which solidified over a period of time, mp 107-112 °C. 3-Bromo-5-methoxv- -dimethvl-4-[[6-chloro-2-methvl-5nitro-4-ovrimidinvl]oxv]benzenemethanol 3-Bromo-4-hydroxy-5-methoxy- -dimethylbenzenemethanol (l.16g) was dissolved in 10% NaOH (1.78g) and 5mL of water. The solvent was stripped under reduced pressure. The salt was taken up in 50mL acetonitrile and added dropwise by pipette to an already cooled solution (0 -5 °C) of 4,6-dichloro-2-methyl-5-nitro-l,3-pyrimidine (0.92g) in 80mL of acetonitrile. The mixture was stirred at 0°-5°C for 3 hours. The solvent was removed under reduced pressure and the residue was extracted with methylene chloride. The extracts were combined and evaporated under reduced pressure to yield the title compound. 3 -Bromo5 -methoxv- - dimet hvl4 - [ [2 -methyl - 5-nitro- - [ ( l-pronvlbutvl ) amino ] -4-Dvrimidinvl ] OXV] benzenemethanol To a solution of 3-bromo-5-methoxy- -dimethyl-4-[[6chloro-2-methyl-5-nitro-4pyrimidinyl]oxy]benzenemethanol (1.88g) in anhydrous 1,4-dioxane (50mL) with 0.50g of potassium carbonate, 4-heptylamine (l.00mL) was added and the solution was stirred at room temperature for 2 hours. The solvent was removed under reduced pressure and the residue was taken up in water and extracted with methylene chloride. The extracts were combined and dried over MgS0 4 . The solvent was removed under reduced pressure and the residue was purified by chromatography on silica gel using a i:i mixture of ethyl acetate and hexane to yield the title compound, mp 138 °C. 3-Bromo-5-methoxy- -dimethyl-4-[(6-(l-methoxypropyl)amino-2-methyl-5-nitro)-4-pyrimidinyl]- oxybenzenemethanol, m.p. 119-120 0C, was prepared by the same procedure. 3-Bromo-5-methoxv- -dimethvl-4-[[5-amino-2-methvl-6- [{l-Dronvlbutvl)amino]-4-nvrimidinvl]oxv]benzenemethanol Platinum black,(5%,0.25g) was added to a solution of 3bromo-5-methoxy- -dimethyl-4-[[2-methyl-5-nitro-6-[(lpropyl-butyl)amino]-4-pyrimidinyl]oxy]benzenemethanol (0.80g) in 50mL of ethanol. The mixture was hydrogenated at a pressure of 41 psi for 18 hours. The mixture was filtered through celite and the filtrate was stripped under reduced pressure. The residue was taken up in IN Na0H and extracted with methylene chloride. The combined methylene chloride extracts were dried over MgSO 4 and the filtrate was stripped under reduced pressure to yield the title compound, mp 114-116 0C. 3-Bromo5-methoxv- -dimethvl-4- [ (5-methyl3- (1pron_vlbutvl I - 3H-I. 2.3 -triazolo [4.5-d] Dvrimidi - 7-vl ) - oxv] benzenemethanol To a solution of 3-bromo-5-methoxy- -d.imethy!-4-[[5amino-2-methyl-6-[(l-propylbutyl)amino]-4pyrimidinyl]oxy]benzenemethanol (0.70g) in 35mL of glacial acetic acid, 0.10g of sodium nitrite in imL of water was added dropwise. The mixture was stirred at room temperature for 20 minutes and then diluted with water, basified with IN NaOH and extracted three times with ethyl acetate. The combined extracts were dried over MgS0 4 and stripped of the solvent under reduced pressure to yield the title compound as viscous liquid. 7- [2-Bromo6-methoxv4- I l-methvlethenvl ) nhenoxy] -5methyl-3 - { l-nronvlbutvl ) -3Hi. 2.3 - riazolo [ 4.5d] Dvrimidine To a solution of 3-bromo-5-methoxy-( -dimethyl-4-[ (5methyl3 - ( l-propylbutyl ) - 3HI, 2,3 - triazolo [ 4,5d]pyrimidin-7-yl)-oxy]benzenemethanol (0.59g) in 35mL of benzene, a small quantity of p-toluene sulfonic acid was added. The solution was refluxed under azeotropic conditions for 1.5 hours. Once cooled to room temperature, the solution was washed with saturated NaHC0 3 followed by water. The organic phase was dried over MgS0 4 and the solvent was removed under reduced pressure. The residue was chromatographed silica gel using a mixture of i:I ethyl acetate and hexane to yield the title compound as a colorless solid, mp 110-115 0C. azamZ a 7 - [ 2 - Bromo6 -methoxv4- l-methyl ethyl ) ohenoxy ] - 5-methyl - 3C I-DroDvlbutvl ) -3H-I. 2.3-triazolo [4.5-d] pyrimidine Platinum black, 5% (0.19g) was added to a solution of 7- [2-bromo-6-methoxy-4-(l-methylethenyl)phenoxy]-5-methyl3-(l-propylbutyl)-3H-l,2,3-triazolo[4,5-d]pyrimidine (0.17g) in 50mL of ethanol. The mixture was hydrogenated at a pressure of 40 psi for 18 hours and filtered through celite. The filtrate was stripped of the solvent under reduced pressure and the residue recrystallized from hexane to yield the title compound as a colorless crystalline solid, mp 129-131 0C. EzamZm__% 3-(l-Ethvloroovl)-5-methvl-7-(2.4.6-trimethvlphenoxv)- 3H-l.2.3-triazolo[4.5-d]pyrimidine 2,4,6-Trimethylphenol (0.114) was added to a solution of sodium methoxide (0.334 g) methanol (I0 mL) and the resulting solution was evaporated to dryness under reduced pressure. The salt thus obtained was taken up in 10mL of acetonitrile and added dropwise by to a cold solution (0-5 °C) of 7-chloro-3-(l-ethylpropyl)-5methyl-3H-l,2,3-triazolo[4,5-d]pyrimidine in 35mL of acetonitrile, such that the temperature did not rise above 5oc. The mixture was stirred at 0-5oc for 3 hours. The solvent was then removed from the mixture under reduced pressure and the residue treated with water and extracted three times with methylene chloride. The combined extracts were dried over MgSO 4 and stripped of the solvent under reduced pressure. The material was purified on silica gel using a solution of 1% methanol in methylene chloride to yield the title compound as a colorless powder, mp 92 °C. 6-{l-Methoxvnroovl)amino-2-methvl-5-nitro-4-[C2-bromo6-methoxv-4-{l-methvlethenvl}ohenoxv]ovrimidine, A few crystals of 4-toluenesulfonic acid were added to a solution of 3-bromo-5-methoxy-a,a-dimethyl-4-[[6-(l- methoxypropyl)amino-2-methyl-5-nitro]-pyrimidinyl]]oxybenzenemethanol (1.70 g) in benzene (30 ml) and the resulting mixture was heated overnight under reflux using Dean-Stark trap. It was then cooled diluted with benzene (70 mL), washed sucessively with IN aq. NaOH and water, dried over magnesium sulfate and evaporated to dryness underreduced pressure to yield a semi solid which upon trituration with ether and filtration yielded a yellow solid. Recrystallization from ethanol furnished the title compound as a light yellow crystalline solid, m.p. 136-137 °C. 2 -Amino6- ( Imet hoxvnronvl ) amino2 -met hvl4- [ { 2 - bromo6 - methoxv-4I l-meth_vlethvl ) Dhenoxv] Dvrimidine Platinum black (5%, 250 mg) was added carefully to a solution of 6-(l-methoxypropyl)amino-2-methyl-5-nitro-4- [ ( 2 -bromo6-methoxy4 ( l-methylethenyl ) phenoxy] pyrimidine (550 mg) in ethyl acetate (i00 mL) and the resulting mixture was hydrogenated at 30 p.s.i, overnight. The mixture was then filtered through a pad of celite and the filtrate evaporated to dry ness under reduced pressure to yield the title com-pound as a highly viscous liquid. Example 12 7 - [ 2 -Bromo6 -methoxv3 - C l-met hoxvnroDvl ) - 5-methyl4- { 1methvlethvl ) ohenoxv] -3H-I, 2.3-triazolo [4,5-d] D_vrimidine A solution of of sodium nitrite (42 mg) in water (i mL) was added dropwise to a solution of 2-amino-6-(lmethoxypropyl)- amino-2-methyl-4-[(2-bromo-6-methoxy-4- (l-methylethyl)- phenoxy]pyrimidine (270 mg) in acetic acid (i0 mL) with stirring at room temperature. After the addititon was complete, the mixture was stirred overnight at room temperature over night and stripped of most of the acetic acid under reduced pressure. The residue was treated with IN aq. NaOH and extracted with ethyl acetate (2X). The ethyl acetate extract was was washed with water, dried over magnesium sulfate and evaporated to dryness under reduced pressure to yield a semi-solid which was chromatographed over silica using i:i ethyl acetate:hexane as the eluent to furnish the title compound, m.p. 149-150 oC. CRF-RI Receptor Binding Assay for the Evaluation of Biological Activity The following is a description of the isolation of cell membranes containing cloned human CRFR1 receptors for use in the standard binding assay as well as a description of the assay itself. Messenger RNA was isolated from human hippocampus. The mRNA was reverse transcribed using oligo (dt) 12-18 and the coding region was amplified by PCR from start to stop codons The resulting PCR fragment was cloned into the EcoRV site of pGEMV, from whence the insert was reclaimed using XhoI + XbaI and cloned into the XhoI + XbaI sites of vector pm3ar ( which contains a CMV promoter, the SV40 't' splice and early poly A signals, an Epstein-Barr viral origin of replication, and a hygromycin selectable marker). The resulting expression vector, called phchCRFR was transfected in 293EBNA cells and cells retaining the episome were selected in the presence of 400 M hygromycin. Cells surviving 4 weeks of selection in hygromycin were pooled, adapted to growth in suspension and used to generate membranes for the binding assay described below. Individual aliquots containing approximately 1 x 108 of the suspended cells were then centrifuged to form a pellet and frozen. For the binding assay a frozen pellet described above containing 293EBNA cells transfected with hCRFRI receptors is homogenized in i0 ml of ice cold tissue buffer ( 50 mM HEPES buffer pH 7.0, containing i0 mM MgCI2, 2 mM EGTA, 1 g/l aprotinin, 1 g/ml leupeptin and 1 Bg/ml pepstatin). The homogenate is centrifuged at 40,000 x g for 12 min and the resulting pellet rehomogenized in i0 ml of tissue buffer. After another centrifugation at 40,000 x g for 12 min, the pellet is resuspended to a protein concentration of 360 g/ml to be used in the assay. Binding assays are performed in 96 well plates; each well having a 300 I capacity. To each well is added 50 i of test drug dilutions (final concentration of drugs range from i0-I0 - 10-5 M), i00 i of 125Iovine-CRF (125I-o-CRF) (final concentration 150 pM) and 150 I of the cell homogenate described above. Plates are then allowed to incubate at room temperature for 2 hours before filtering the incubate over GF/F filters (presoaked with 0.3% polyethyleneimine) using an appropriate cell harvester. Filters are rinsed 2 times with ice cold assay buffer before removing individual filters and assessing them for radioactivity on a gamma counter. Curves of the inhibition of 125I-o-CRF binding to cell membranes at various dilutions of test drug are analyzed by the iterative curve fitting program LIGAND [P.J. Munson and D. Rodbard, Anal. Biochem. 107:220 (1980), which provides Ki values for inhibition which are then used to assess biological activity. A compound is considered to be active if it has a Ki value of less than about i0000 nM for the inhibition of CRF to its receptor. Inhibition of CRF-Stimulated Adenvlate Cvclase Activity Inhibition of CRF-stimulated adenylate cyclase activity was performed as described by G. Battaglia et al. Synapse 1:572 (1987). Briefly, assays were carried out at 37° C for i0 min in 200 ml of buffer containing i00 mM Tris-HCl (pH 7.4 at 37° C), i0 mM MgCI2, 0.4 mM EGTA, 0.1% BSA, 1 mM isobutylmethylxanthine (IBMX), 250 units/ml phosphocreatine kinase, 5 mM creatine phosphate, i00 mM guanosine 5'-triphosphate, i00 nM oCRF, antagonist peptides (concentration range 10-9 to I0-6m) and 0.8 mg original wet weight tissue (approximately 40-60 mg protein). Reactions were initiated by the addition of 1 mM ATp/32p]ATP (approximately 2-4 mCi/tube) and terminated by the addition of i00 ml of 50 mM TrisHCL, 45 mMATP and 2% sodium dodecyl sulfate. In order to monitor the recovery of cAMP, 1 i ofcAMP (approximately 40,000 dpm) was added to each tube prior to separation. The separation ofcAMP fromATP was performed by sequential elution over Dowex and alumina columns. Recovery was consistently greater than 80%. Some compounds of this invention were tested in this assay and found to be active. Is vivo Biological Assay The in vivo activity of the compounds of the present invention can be assessed using any one of the biological assays available and accepted within the art. Illustrative of these tests include the Acoustic Startle Assay, the Stair Climbing Test, and the Chronic Administration Assay. These and other models useful for the testing of compounds of the present invention have been outlined in C.W. Berridge and A.J. Dunn Brain Research Reviews 15:71 (1990) Compounds may be tested in any species of rodent or small mammal. Disclosure of the assays herein is not intended to limit the enablement of the invention. The compounds of this invention have utility in the treatment of inbalances associated with abnormal levels of corticotropin releasing factor in patients suffering from depression, affective disorders, and/or anxiety. Compounds of this invention can be administered to treat these abnormalities by means that produce contact of the active agent with the agent's site of action in the body of a mammal. The compounds can be administered by any conventional means available for use in conjunction with pharmaceuticals either as individual therapeutic agent or in combination of therapeutic agents. They can be administered alone, but will generally be administered with a pharmaceutical carrier selected on the basis of the chosen route of administration and standard pharmaceutical practice. The dosage administered will vary depending on the use and known factors such as pharmacodynamic character of the particular agent, and its mode and route of administration; the recipient's age, weight, and health; nature and extent of symptoms; kind of concurrent treatment; frequency of treatment; and desired effect. For use in the treatment of said diseases or conditions, the compounds of this invention can be orally administered daily at a dosage of the active ingredient of 0.002 to 200 mg/kg of body weight. Ordinarily, a dose of 0.01 to I0 mg/kg in divided doses one to four times a day, or in sustained release formulation will be effective in obtaining the desired pharmacological effect. Dosage forms (compositions) suitable for administration contain from about 1 mg to about i00 mg of active ingredient per unit. In these pharmaceutical compositions, the active ingredient will ordinarily be present in an amount of about 0.5 to 95% by weight based on the total weight of the composition. The active ingredient can be administered orally is solid dosage forms, such as capsules, tablets and powders; or in liquid forms such as elixirs, syrups, and/or suspensions. The compounds of this invention can also be administered parenterally in sterile liquid dose formulations. Gelatin capsules can be used to contain the active ingredient and a suitable carrier such as but not limited to lactose, starch, magnesium stearate, steric acid, or cellulose derivatives. Similar diluents can be used to make compressed tablets. Both tablets and capsules can be manufactured as sustained release products to provide for continuous release of medication over atperiod of time. Compressed tablets can be sugar-coated or film-coated to mask any unpleasant taste, or used to protect the active ingredients from the atmosphere, or to allow selective disintegration of the tablet in the gastrointestinal tract. Liquid dose forms for oral administration can contain coloring or flavoring agents to increase patient acceptance. In general, water, pharmaceutically acceptable oils, saline, aqueous dextrose (glucose), and related sugar solutions and glycols, such as propylene glycol or polyethylene glycol, are suitable carriers for parenteral solutions. Solutions for parenteral administration preferably contain a water soluble salt of the active ingredient, suitable stabilizing agents, and if necessary, butter substances. Antioxidizing agents, such as sodium bisulfite, sodium sulfite, or ascorbic acid, either alone or in combination, are suitable stabilizing agents. Also used are citric acid and its salts, and EDTA. In addition, parenteral solutions can contain preservatives such as benzalkonium chloride, methyl- or propyl-paraben, and chlorobutanol. Suitable pharmaceutical carriers are described in "Remington's Pharmaceutical Sciences", A. Osol, a standard reference in the field. Useful pharmaceutical dosage-forms for administration of the compounds of this invention can be illustrated as follows: A large number of units capsules are prepared by filling standard two-piece hard gelatin capsules each with i00 mg of powdered active ingredient, 150 mg lactose, 50 mg cellulose, and 6 mg magnesium stearate. soft Gelatin Cansu]es A mixture of active ingredient in a digestible oil such as soybean, cottonseed oil, or olive oil is prepared and injected by means of a positive displacement was pumped into gelatin to form soft gelatin capsules containing 100 mg of the active ingredient. The capsules were washed and dried. A large number of tablets are prepared by conventional procedures so that the dosage unit was i00 mg active ingredient, 0.2 mg of colloidal silicon dioxide, 5 mg of magnesium stearate, 275 mg of microcrystalline cellulose, ii mg of starch, and 98.8 mg lactose. Appropriate coatings may be applied to increase palatability or delayed adsorption. The compounds of this invention may also be used as reagents or standards in the biochemical study of neurological function, dysfunction, and disease. Where the terms "comprise", "comprises", "comprised" or "comprising" are used in this specification, they are to be interpreted as specifying the presence of the stated features, integers, steps or components referred to, but not to preclude the presence or addition of one or more other feature, integer, step, component or group thereof.