WO2000055137A1 - Compounds and methods for modulation of estrogen receptors - Google Patents
Compounds and methods for modulation of estrogen receptors Download PDFInfo
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- WO2000055137A1 WO2000055137A1 PCT/US2000/007109 US0007109W WO0055137A1 WO 2000055137 A1 WO2000055137 A1 WO 2000055137A1 US 0007109 W US0007109 W US 0007109W WO 0055137 A1 WO0055137 A1 WO 0055137A1
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- 0 CCC(CCC1)C(CC2=CC=CC(C)(C)C=C2)C2=C1C=C*(C1CCCC1)C=C2 Chemical compound CCC(CCC1)C(CC2=CC=CC(C)(C)C=C2)C2=C1C=C*(C1CCCC1)C=C2 0.000 description 9
- HEMCGZPSGYRIOL-UHFFFAOYSA-N C(C1)C11CCCC1 Chemical compound C(C1)C11CCCC1 HEMCGZPSGYRIOL-UHFFFAOYSA-N 0.000 description 1
- SWTYYQMHPNFSLD-UHFFFAOYSA-N CC(C)N(CCCCc1ccc(CC(c2ccc(C3CC3)cc2CC2)N2c(cc2)ccc2F)cc1)C(C)C Chemical compound CC(C)N(CCCCc1ccc(CC(c2ccc(C3CC3)cc2CC2)N2c(cc2)ccc2F)cc1)C(C)C SWTYYQMHPNFSLD-UHFFFAOYSA-N 0.000 description 1
- TXFPEBPIARQUIG-UHFFFAOYSA-N CC(c(cc1)ccc1O)=O Chemical compound CC(c(cc1)ccc1O)=O TXFPEBPIARQUIG-UHFFFAOYSA-N 0.000 description 1
- AQSKKIQGEFFSMF-UHFFFAOYSA-N CC(c(cc1)ccc1OCC[Br]=C)=O Chemical compound CC(c(cc1)ccc1OCC[Br]=C)=O AQSKKIQGEFFSMF-UHFFFAOYSA-N 0.000 description 1
- WTKFZCIQMULZRN-UHFFFAOYSA-N Oc1ccc(C(Cc(cc2)ccc2OCCCC2CCCCC2)N(CC2)c(ccc(Cl)c3)c3O)c2c1 Chemical compound Oc1ccc(C(Cc(cc2)ccc2OCCCC2CCCCC2)N(CC2)c(ccc(Cl)c3)c3O)c2c1 WTKFZCIQMULZRN-UHFFFAOYSA-N 0.000 description 1
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Definitions
- This invention is generally directed to estrogen antagonists and agonists, including pharmaceutical compositions and uses thereof, and more specifically to compounds which selectively modulate estrogen receptor-beta (ER- ⁇ ) activity.
- ER- ⁇ estrogen receptor-beta
- the estrogen hormone has a broad spectrum of effects on tissues in both females and males. Many of these biological effects are positive, including maintenance of bone density, cardiovascular protection, central nervous system (CNS) function, and the protection of organ systems from the effects of aging. However, in addition to its positive effects, estrogen also is a potent growth factor in breast and endometrium that increases the risk of cancer.
- estrogen binds to a single estrogen receptor (ER) in cells, causing conformational changes that result in release from heat shock proteins and binding of the receptor as a dimer to the so-called estrogen response element in the promoter region of a variety of genes.
- pharmacologists have generally believed that non-steroidal small molecule ligands compete for binding of estrogen to ER, acting as either antagonists or agonists in each tissue where the estrogen receptor is expressed. Thus, such ligands have traditionally been classified as either pure antagonists or agonists. This is no longer believed to be correct.
- ER associates with co- activators (e.g., SRC-1, CBP and SRA) and co-repressors (e.g., SMRT and N-CoR) that modulate the transcriptional activity of ER in a tissue-specific and ligand-specific manner.
- co- activators e.g., SRC-1, CBP and SRA
- co-repressors e.g., SMRT and N-CoR
- SERM selective estrogen receptor modulator
- ER- ⁇ and the classical ER renamed ER- ⁇ , have significantly different amino acid sequences in the ligand binding domain and carboxy-terminal transactivation domains (-56% amino acid identity), and only 20% homology in their amino-terminal transactivation domain. This suggests that some ligands may have higher affinity to one receptor over the other. Further, ligand-dependent conformational changes of the two receptors, and interaction with co-factors, will result in very different biological actions of a single ligand.
- a ligand that acts as an agonist on ER- ⁇ may very well serve as an antagonist on ER- ⁇ .
- An example of such behavior has been described by Paech et al. (Science 277, 1508-1510, 1997).
- estrogen is reported to activate an AP-1 site in the presence of ER- ⁇ , but to inhibit the same site in the presence of ER- ⁇ .
- Raloxifene Eli Lilly & Co.
- Tamoxifen and ICI- 182,780 Zeneca Pharmaceuticals
- ER- ⁇ and ER- ⁇ have both overlapping and different tissue distributions, as analyzed predominantly by RT-PCR or in-situ hybridization due to a lack of good ER- ⁇ antibodies. Some of these results, however, are controversial, which may be attributable to the method used for measuring ER, the species analyzed (rat, mouse, human) and/or the differentiation state of isolated primary cells. Very often tissues express both ER- ⁇ and ER- ⁇ , but the receptors are localized in different cell types.
- tissues such as kidney
- tissues such as uterus, pituitary and epidymis
- ER- ⁇ ER- ⁇
- tissues expressing high levels of ER- ⁇ include prostate, testis, ovaries and certain areas of the brain (Brandenberger et al., J. Clin. Endocrinol Metab. 83, 1025-8, 1998; Enmark et al., J. Clinic.
- knockout mice further demonstrate that ER- ⁇ has different functions in different tissues.
- ER- ⁇ knockout mice male and female are infertile, females do not display sexual receptivity and males do not have typical male-aggressive behavior (Cooke et al., Biol Reprod. 59, 470-5, 1998; Das et al., Proc. Natl. Acad. Sci. USA 94, 12786-12791, 1997; Korach, 1994; Ogawa et al., Proc. Natl. Acad. Sci.
- mice lacking the ER- ⁇ develop normally, are fertile and exhibit normal sexual behavior, but have fewer and smaller litters than wild-type mice (Krege et al., 1998), have normal breast development and lactate normally.
- the reduction in fertility is believed to be the result of reduced ovarian efficiency, and ER- ⁇ is the predominant form of ER in the ovary, being localized in the granulosa cells of maturing follicles.
- ER- ⁇ knockout mice display signs of prostatic hyperplasia with aging, which suggests that ER- ⁇ may normally protect against abnormal growth (Krege et al., 1998).
- ER- ⁇ /ER- ⁇ double knockout mice are viable, but infertile, and display a postnatal reversal of the ovaries (Couse et al., Science 286, 2328-2331 , 1999).
- breast and non-breast cancer cells have been described to express ER, and serve as the target tissue for specific estrogen antagonists (Brandenberger et al., 1998; Clinton and Hua, Crit. Rev. Oncol Hematol. 25, 1-9, 1997; Hata et al., Oncology 55 Suppl 1, 35-44, 1998; Rohlff et al., Prostate 37, 51-9, 1998; Simpson et al, J Steroid Biochem Mol Biol 64, 137-45,1998; Yamashita et al., Oncology 55 Suppl 1, 17-22, 1998).
- ER-selective modulators would similarly possess significant clinical utility. Since ER- ⁇ is expressed strongly in a number of tissues including prostrate, bladder, ovary, testis, lung, small intestine, vascular endothelium, and various parts of the brain, compounds that selectively modulate ER- ⁇ would be of clinical importance in the treatment of a variety of diseases or conditions, such as prostate cancer, testicular cancer, cardiovascular diseases, neurodegenerative disorders, urinary incontinence, CNS, GI tract conditions, and bone and other cancers. Such compounds would have minimal effect on tissues that contains ER- ⁇ , and thus exhibit different side-effect profiles.
- estrogen replacement therapy is associated with a variety of beneficial effects (such as bone protection, cardiovascular effect, prevention of hot flashes, dementia, bone metabolism, etc.), such therapy also has adverse effects (such as breast and endometrial cancer, thrombosis, etc.). Some of these adverse effects .are believed to be mediated by ER- ⁇ or ER- ⁇ specific mechanisms.
- ER- ⁇ antagonists or agonists will display different therapeutic profiles compared to ER- ⁇ antagonists or agonists, and would be preferentially beneficial in tissues expressing high levels of ER- ⁇ (see, e.g., Nilsson et al., TEM 9, 387-395, 1998; Chang and Prins, The Prostate 40, 1 15-124, 1999).
- the present invention is generally directed to estrogen antagonists and/or agonists, including pharmaceutical compositions containing the same, as well as to methods for treating estrogen-related conditions.
- Such conditions are more specifically discussed below, and generally include (but are not limited to) obesity, breast cancer, osteoporosis, endometriosis, cardiovascular disease, prostate cancer, menopausal syndromes, hair loss (alopecia), type-II diabetes, Alzheimer's disease, urinary incontinence, GI tract conditions, spermatogenesis, vascular protection after injury, endometriosis, learning and memory, CNS effects, plasma lipid levels, acne, cataracts, hirsutism, other solid cancers (such as colon, lung, ovarian, testis, melanoma, CNS, and renal), multiple myeloma, and lymphoma.
- estrogen antagonists and/or agonists of this invention are compounds having the following structure (I):
- compositions including stereoisomers and pharmaceutically acceptable salts thereof, wherein A, B, C, D, R), Ps. 2 , R 3 and a are as identified in the following detailed description.
- pharmaceutical compositions are also disclosed containing one or more compounds of structure (I), in combination with a pharmaceutically acceptable carrier or diluent.
- methods are disclosed for modulating cells and/or tissues that express ER- ⁇ by contacting the cell and/or tissue with an effective amount of a compound of structure (I).
- the cell and/or tissue preferentially expresses ER- ⁇ over ER- ⁇ , such as cell and/or tissue of bone, bladder, uterus, ovary, prostate, testis, epididymis, gastrointestinal (GI) tract, kidney, breast, heart, vessel wall, immune system, lung, pituitary, hippocampus and hypothalamus.
- ER- ⁇ ER- ⁇ over ER- ⁇
- the present invention discloses methods for treating an estrogen-related condition by administering to an warm-blooded animal in need thereof an effective amount of a compound of structure (I) formulated as a pharmaceutical composition suitable for administration to the animal.
- the estrogen-related condition is breast cancer, osteoporosis, endometriosis, cardiovascular disease, hypercholesterolemia, prostatic hypertrophy, obesity, prostate cancer, menopausal syndromes, type-II diabetes, Alzheimer's disease, urinary incontinence, GI tract conditions, spermatogenesis, vascular protection after injury, endometriosis, learning and memory, CNS effects, plasma lipid levels, acne, hirsutism, other solid cancers (such as colon, lung, ovarian, testis, melanoma, CNS, and renal), multiple myeloma, lymphoma, prostatic carcinomas, obesity, hot flashes, skin effects, mood swings, memory loss, and/or adverse reproductive effects associated with exposure to environmental chemicals.
- methods are disclosed for inhibiting a cyctokine, such as IL-6 and GM-CSF, in an animal in need thereof, as well as methods for treating cancer associated therewith.
- Figures 1A and IB illustrate proliferation of Tamoxifen resistant LCC1 and LCC2 breast cancer cell lines when exposed to a representative compound of this invention.
- the present invention is directed to compounds that have activity as estrogen antagonists and/or agonists, as well as pharmaceutical compositions containing one or more of such compounds and methods related to the same.
- the compounds of this invention have utility in the treatment of a wide range of estrogen-related conditions.
- the term "treatment” includes both treatment and/or prevention of an estrogen-related condition.
- the compounds of this invention may be administered as a therapeutic and/or prophylactic agent.
- An estrogen "agonist” is a compound that binds to ER and mimics the action of estrogen in one or more tissues, while an “antagonist” binds to ER and blocks the action of estrogen in one or more tissues.
- the term “estrogen- related condition” encompasses any condition associated with elevated or depressed levels of estrogen, a selective estrogen receptor modulators (SERM), ER- ⁇ or ER- ⁇ .
- SERM selective estrogen receptor modulators
- the compounds of the present invention may also be used within a method for treating estrogen-related conditions, including (but not limited to) breast cancer, osteoporosis, . endometriosis, cardiovascular disease, hypercholesterolemia, prostatic hypertrophy, prostatic carcinomas, obesity, hot flashes, skin effects, mood swings, memory loss, menopausal syndromes, hair loss (alopecia), type-II diabetes, Alzheimer's disease, urinary incontinence, GI tract conditions, spermatogenesis, vascular protection after injury, endometriosis, learning and memory, CNS effects, plasma lipid levels, acne, hirsutism, other solid cancers (such as colon, lung, ovarian, testi, melanoma, CNS, and renal), multiple myeloma, cataracts, lymphoma, and adverse reproductive effects associated with exposure to environmental chemicals.
- estrogen-related conditions including (but not limited to) breast cancer, osteoporosis, . endometriosis, cardiovascular disease,
- the compounds of this invention are selective estrogen receptor modulators and, more specifically, are selective to ER- ⁇ . Accordingly, in this aspect of the invention, the compounds have utility as agents for treatment of osteoporosis, hormonally regulated cancer, combination treatment of cancer (such as with taxol cisplatin or chemotherapy), women's gynecologic health issues, and health conditions resulting from exposure to environmental chemicals.
- the compounds of this invention have the following structure (I):
- A, B and C are independently CH, CR or N;
- Ri represents one or two substituents independently selected from -X-Y;
- R 5 , Rs, R and R 8 are at each occurrence independently hydrogen
- Y is at each occurrence independently halogen; -Re;
- G is O, S or NR e ; n and m are at each occurrence independently 0, 1, 2 or 3; p is at each occurrence independently 1, 2 or 3; q is at each occurrence independently 0, 1 or 2; r is at each occurrence independently 1, 2, 3, 4 or 5; s is at each occurrence independently 0, 1, 2, 3 or 4; R is at each occurrence independently C ⁇ - 6 alkyl;
- R a and R D are at each occurrence independently C ⁇ - 8 alkyl or taken together form a C 3 - cyclic alkyl;
- R e and Rj are at each occurrence independently hydrogen or C ⁇ . 4 alkyl; and R e and R f are at each occurrence independently hydrogen, C 6 -i 2 aryl,
- Halogen means F, CI, Br and I.
- C,. 4 alkyl means a straight chain or branched, cyclic or non-cyclic, saturated or unsaturated carbon chain having from 1 to 4, 6 or 8 carbon atoms, respectively.
- the C ⁇ - ⁇ alkyl (where X is 4, 6 or 8 as disclosed above) is a fully saturated, straight chain alkyl such as methyl, ethyl, n-propyl, n-butyl, n-pentyl, n-hexyl and the like.
- the C is a fully saturated, straight chain alkyl such as methyl, ethyl, n-propyl, n-butyl, n-pentyl, n-hexyl and the like.
- the C ].
- ⁇ alkyl is a fully saturated cyclic alkyl such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and the like, or an alkyl(cycloalkyl) moiety such .as methylenecyclopropyl, methylenecyclobutyl, methylenecyclopentyl, methylenecyclohexyl, and the like, or an unsaturated cyclic alkyl.
- the C ⁇ - X alkyl is a fully saturated, branched alkyl such as iso-propyl, iso-butyl, tert-butyl, iso-pentyl, iso-hexyl, and the like.
- the -x alkyl is an unsaturated straight chain alkyl such as ethylenyl, propylenyl, 1-butenyl, 1-pentenyl, 1-hexenyl, and the like.
- C 6 - ⁇ 2 aryl means a carbocyclic aromatic moiety containing from 6 to 12 carbon atoms.
- the C 6 -i2aryl is phenyl, tetralinyl or napthalenyl, and typically is phenyl.
- C -i 2 aralkyl means an arene containing from 7 to 12 carbon atoms, and has both aliphatic and aromatic components.
- the C 7 . 12 aralkyl is benzyl, ethylenephenyl, propylenephenyl, and the like.
- “Five- or six-membered heterocycle” means a heterocyclic ring containing up to two heteroatoms selected from O, NR c and S(O) ? , and wherein the number of carbon and heteroatoms of the ring total 5 or 6, including both saturated and unsaturated, aromatic and non-aromatic ring systems, such as pyridinyl, pyrimidinyl, furanyl, thienyl, triazenyl, imidazolyl, thiazolyl, pyrazolyl, pyridazinyl, pyrazinyl, and the like.
- “Five- or six-membered heterocyclealkyl” means a C ⁇ - 6 alkyl having at least one hydrogen replaced with a five- or six-membered heterocyle, such as -CH (hererocycle), and the like.
- Ci- .t alkoxy means a -O(C ⁇ - alkyl), where x is 4, 6 or 8.
- C ⁇ -- t thio means -SC ⁇ - alkyl.
- Ci- alkylsulfinyl means -SOC ⁇ - alkyl.
- C ⁇ _ ⁇ alkylsulfonyl means • S ⁇ 2 C ⁇ - alkyl.
- (hydroxy)Cj- 4 alkyl means C ⁇ --,alkyl wherein a hydrogen atom has been substituted by hydroxyl.
- _,alkylamino means -NHC,- 4 alkyl.
- C ⁇ --dialkylammo means -N(C ⁇ - alkyl)( C ⁇ - alkyl).
- C ⁇ -thaloalkyl means a C ⁇ _ alkyl having at least one hydrogen replaced with halogen, such as trifluoromethyl and the like.
- a and B are both CH, C is N, D is -CH 2 -, and the compounds of this invention have the following structure (IJa) when a is 1, (Lib) when a is 0, and (lie) when a is 2:
- the compounds of structure (I) have the following structures (III), (IV), (V) or (VI):
- R 2 is phenyl optionally substituted with one, two or three substituents independently selected from R 4 , R 3 is hydrogen, and the compounds of this invention have the following structure (IIa-1):
- R 2 is pyridinyl optionally substituted with one, two or three substituents independently selected from R- t , R 3 is hydrogen, and the compounds of this invention have the following structures (IIa-2) or (IIa-3):
- Ri is a the 4-position
- R 3 is hydrogen
- the compounds of this invention have the following structure (IIa-4):
- the compounds of this invention have the following structure (IIa-5) or (IIa-6):
- the compounds of this invention have the following structure (IIa-7):
- compounds of this invention have the following structure (Nil):
- R 3 is hydrogen and compounds of this invention have the following structure (Villa):
- D of structure (I) is -(CH 2 ) r - and the compounds of this invention have the following structure (IX):
- R 3 is hydrogen and compounds of this invention have the following structure (IXa):
- compounds of this invention have structure (I), wherein a is 1, 2 or 3, yielding a fused, bicyclic six-five-, six-six- or six-seven-membered ring system.
- a is 1.
- both A and B are CH, yielding a benzene ring substituted with the Ri moiety.
- Other representative groups in this regard include those embodiments wherein either A or B is nitrogen, or wherein both A and B are nitrogen.
- Representative C moieties include both nitrogen and CH. In a typical embodiment, the C moiety is nitrogen.
- r is typically 1 or 2, and more typically 1 - such that D moiety is methylene.
- n and m are typically 0, 1 or 2. In one embodiment, both n and m are zero, and D is carbonyl.
- Ri groups of this invention have the formula -X-Y.
- Ri designates either one or two Ri substuents. In the case of two Rj substituents, each of the Ri substituents may be the same or different. Typically. Ri refers to a single substituent as represented by -X-Y.
- X is -(CH 2 ) disguiseZ(CH 2 ) m - and Y has the following structure:
- R ⁇ groups in this regard include those wherein n is zero and Z is oxygen, and having the following structure:
- Ri groups include the following (wherein m is, for example, 2 or 3):
- R ⁇ groups also include those having the following structure:
- R ⁇ is hydrogen, halogen (such as fluorine, bromine or chloribne) or hydroxyl.
- halogen such as fluorine, bromine or chloribne
- R 2 groups include substituted or unsubstitued C 6 -i 2 aryl, and typically substituted phenyl.
- R 2 is phenyl substituted with one or two substituents selected from halogen, such as fluorine.
- further representative R 2 groups include those as set forth below in Examples 1-139.
- R 3 groups include hydrogen and C ⁇ - 4 alkyl, and R 3 is typically hydrogen or methyl.
- the compounds of this invention may be made by the procedures and tecliniques disclosed in the Examples, as well as by known organic synthesis techniques, including the techniques disclosed in published PCT WO 96/21656 (which i D reference is inco ⁇ orated herein in its entirety) but utilizing the corresponding benzyl starting materials rather than the phenyl compounds.
- the compounds of this invention may be made by the following general reaction schemes.
- compounds of structure (I) where D is carbonyl may be made according to the above reaction scheme.
- Ketone (x) is oxidized with selenium dioxide to yield the glyoxal (y).
- Treatment of (y) with secondary amine (z) and trifluoroacetic acid provides compounds of structure (I) wherein D is carbonyl, which can be converted to the corresponding hydroxyl (aa) by d ⁇ benzylation using hydrogen and palladium on carbon.
- the above Reaction Scheme 7 illustrates the synthesis of compounds of structure (I) wherein a is 0.
- the dihydroisobenzofuran (bb) is prepared as described by Sakamoto et al. (Chem. Pharm. Bull. 31, 2698-2707, 1983).
- Treatment of (bb) with aldehyde (cc) provides the adduct (dd), which upon reaction with primary amine (b) yields the isoindolinone (ee).
- the double bond of (ee) is reduced using hydrogen and palladium on carbon to yield the corresponding isoindolinone (ff).
- esters and salts may be prepared from certain compounds of this invention. All of such stereoisomers, esters and salts are included in this invention.
- the methods for treating estrogen-related conditions of this invention include administration of an effective amount of a compound of structure (I), or a salt or ester thereof, as the active ingredient.
- salts of the compounds of structure (I) are typically salts of non-toxic type commonly used, such as salts with organic acids (e.g., formic, acetic, trifluoroacetic, citric, maleic, tartaric, methanesulfonic, benzenesulfonic or toluenesulfonic acids), inorganic acids (e.g., hydrochloric, hydrobromic, sulfuric or phosphoric acids), and amino acids (e.g., aspartic or glutamic acids).
- organic acids e.g., formic, acetic, trifluoroacetic, citric, maleic, tartaric, methanesulfonic, benzenesulfonic or toluenesulfonic acids
- inorganic acids e.g., hydrochloric, hydrobromic, sulfuric or phosphoric acids
- amino acids e.g., aspartic or glutamic acids
- Suitable formulations may be prepared by methods commonly employed using conventional, organic or inorganic additives, such as an excipient (e.g., sucrose, starch, mannitol, sorbitol, lactose, glucose, cellulose, talc, calcium phosphate or calcium carbonate), a binder (e.g., cellulose, methylcellulose, hydroxymethylcellulose, polypropylpyrrolidone, polyvinylprrolidone, gelatin, gum arabic, polyethyleneglycol, sucrose or starch), a disintegrator (e.g., starch, carboxymethylcellulose, hydroxypropylstarch, low substituted hydroxypropylcellulose, sodium bicarbonate, calcium phosphate or calcium citrate), a lubricant (e.g., sucrose, starch, mannitol, sorbitol, lactose, glucose, cellulose, talc, calcium phosphate or calcium carbonate), a binder (e.g., cellulose,
- the active ingredient may be usually administered one to four times a day with a unit dosage of 0.1 mg to 100 or 200 mg in human patients, but the above dosage may be properly varied depending on the age, body weight and medical condition of the patient and the type of administration.
- a preferred dose is 0.25 mg to about 60 mg in human patients.
- One dose per day is preferred.
- the compounds of this invention have utility as estrogen agonists and antagonists, as well as pharmaceutical agents or intermediates thereto.
- estrogen agonists are useful for oral contraception; relief for the symptoms of menopause; prevention of threatened or habitual abortion; relief of dysmenorrhea; relief of dysfunctional uterine bleeding; relief of endometriosis; an aid in ovarian development; treatment of acne; diminution of excessive growth of body hair in women (hirsutism); the prevention and treatment of cardiovascular disease; prevention and treatment of atherosclerosis; prevention and treatment of osteoporosis; treatment of benign prostatic hype ⁇ lasia and prostatic carcinoma obesity; and suppression of post- parturn lactation.
- estrogen antagonists are useful as antiestrogens in, for example, breast and ovarian tissue and thus are useful in the treatment and prevention of breast and ovarian cancer.
- Pharmaceutical chemists will easily recognize that physiologically active compounds which have accessible hydroxy groups are frequently administered in the form of pharmaceutically acceptable esters. The literature concerning such compounds, such as estradiol, provides a great number of instances of such esters. The compounds of this invention are no exception in this respect, and can be effectively administered as an ester, formed on the hydroxy groups, just as one skilled in pharmaceutical chemistry would expect.
- esters are metabolically cleaved in the body, and that the actual drug, which such form is administered, is the hydroxy compound itself. It is possible, as has long been known in pharmaceutical chemistry, to adjust the rate or duration of action of the compound by appropriate choices of ester groups.
- the pharmaceutically acceptable acid addition salts of the compounds of this invention may be formed of the compound itself, or of any of its esters, and include the pharmaceutically acceptable salts which are often used in pharmaceutical chemistry.
- salts may be formed with inorganic or organic acids such as hydrochloric acid, hydrobromic acid, hydroiodic acid, sulfonic acids including such agents as naphthalenesulfonic, methanesulfonic and toluenesulfonic acids, sulfuric acid, nitric acid, phosphoric acid, tartaric acid, pyrosulfuric acid, metaphosphoric acid, succinic acid, formic acid, phthalic acid, lactic acid and the like, most preferable with hydrochloric acid, citric acid, benzoic acid, maleic acid, trifluoroacetate salt, acetic acid and propionic acid. It is usually preferred to administer a compound of this invention in the form of an acid addition salt, as it is customary in the administration of pharmaceuticals bearing a basic group such
- the compounds of this invention are very often administered in the form of acid addition salts.
- the salts are conveniently formed, as is usual in organic chemistry, by reacting the compound of this invention with a suitable acid, such as have been described above.
- the salts are quickly formed in high yields at moderate temperatures, and often are prepared by merely isolating the compound from a suitable acidic wash in the final step of the synthesis.
- the salt-forming acid is dissolved in an appropriate organic solvent, or aqueous organic solvent, such as an alkanol, ketone or ester.
- a typical technique for preparing hydrochlorides is to dissolve the free base in a suitable solvent and dry the solution thoroughly, as over molecular sieves, before bubbling hydrogen chloride gas through it.
- the dose of a compound of this invention to be administered to a human is rather widely variable and subject to the judgment of the attending physician. It should be noted that it may be necessary to adjust the dose of a compound when it is administered in the form of a salt, such as a laureate, the salt forming moiety of which has an appreciable molecular weight.
- the general range of effective administration rates of the compounds is from about 0.05 mg/day to about 200 mg/day.
- a preferred rate range is from about 0.25 mg/day to 60 mg/day.
- the route of administration of the compounds of this invention is not critical.
- the compounds are known to be absorbed from the alimentary tract, and so it is usually preferred to administer a compound orally for reasons of convenience.
- the compounds may equally effectively be administered percutaneously, or as suppositories for abso ⁇ tion by the rectum, if desired in a given instance.
- compositions which are important and novel embodiments of the invention because of the presence of the compounds. All of the usual types of compositions may be used, including tablets, chewable tablets, capsules, solutions, parenteral solutions, troches, suppositories and suspensions. Compositions are formulated to contain a daily dose, or a convenient fraction of daily dose, in a dosage unit, which may be a single tablet or capsule or convenient volume of a liquid.
- any of the compounds may be readily formulated as tablets, capsules and the like; it is preferable to prepare solutions from water-soluble salts, such as the hydrochloride salt.
- water-soluble salts such as the hydrochloride salt.
- all of the compositions are prepared according to methods usual in pharmaceutical chemistry.
- Capsules are prepared by mixing the compound with a suitable diluent and filling the proper amount of the mixture in capsules.
- the usual diluents include inert powdered substances such as starch of many different kinds, powdered cellulose, especially crystalline and microcrystalline cellulose, sugars such as fructose, mannitol and sucrose, grain flours and similar edible powders.
- Tablets are prepared by direct compression, by wet granulation, or by dry granulation. Their formulations usually inco ⁇ orate diluents, binders, lubricants and disintegrators as well as the compound.
- Typical diluents include, for example, various types of starch, lactose, mannitol, kaolin, calcium phosphate or sulfate, inorganic salts such as sodium chloride and powdered sugar. Powdered cellulose derivatives are also useful.
- Typical tablet binders are substances such as starch, gelatin and sugars such as lactose, fructose, glucose and the like. Natural and synthetic gums are also convenient, including acacia, alginates, methylcellulose, polyvinylpyrrolidine and the like. Polyethylene glycol, ethylcellulose and waxes can also serve as binders.
- a lubricant is typically necessary in a tablet formulation to prevent the tablet and punches from sticking in the die.
- the lubricant is chosen from such slippery solids as talc, magnesium and calcium stearate, stearic acid and hydrogenated vegetable oils.
- Tablet disintegrators are substances which swell when- wetted to break up the tablet and release the compound. They include starches, clays, celluloses, algins and gums. More particularly, corn and potato starches, methylcellulose, agar, bentonite, wood cellulose, powdered natural sponge, cation-exchange resins, alginic acid, guar gum, citrus pulp and carboxymethyl cellulose, for example, may be used as well as sodium lauryl sulfate.
- Tablets are often coated with sugar as a flavor and sealant, or with film-forming protecting agents to modify the dissolution properties of the tablet.
- the compounds may also be formulated as chewable tablets, by using large amounts of pleasant-tasting substances such as mannitol in the formulation, as is now well - established in the art.
- the typical bases may be used. Cocoa butter is a traditional suppository base, which may be modified by addition of waxes to raise its melting point slightly.
- Water-miscible suppository bases comprising, particularly, polyethylene glycols of various molecular weights are in wide use. The effect of the compounds may be delayed or prolonged by proper formulation.
- a slowly soluble pellet of the compound may be prepared and inco ⁇ orated in a tablet or capsule.
- the technique may be improved by making pellets of several different dissolution rates and filling capsules with a mixture of the pellets. Tablets or capsules may be coated with a film which resists dissolution for a predictable period of time. Even the parenteral preparations may be made long-acting, by dissolving or suspending the compound in oily or emulsified vehicles which allow it to disperse only slowly in the serum.
- 1,2,3,4-tetrahydroisoquinoline was prepared as described in Example 14.E, using 6- methoxy-2-(2-phenylethyl)-2-(4-hydroxyphenyl)- 1 ,2,3,4-tetrahydroisoquinoline (0.05g,
- Example 44 G, using 2-(4-fluorophenyl)-6-(phenylmethoxy)-l- ⁇ 4-[(2- piperidyl)ethoxy]benzyl ⁇ - 1,2,3,4-tetrahydroisoquinoline (8.4 g, 0.018 mol) to provide the title compound (6.0 g, 87% yield): ES-MS (m/z) 461 [M+H] + .
- C 2-(4-Fluorophenyl)-l-[4-(2-piperidylethoxy)benzyl]-6-l,2,3,4- tetrahydroisoquinolyl methylsulfonat ⁇
- the titl ⁇ compound was prepared as described in Example 56. C, using isobutyric acid (103 ⁇ l, 1.12 mmol) and diisopropylethyl amine (10 ⁇ l, 0.4 mol) to provide the title compound (0.054 g, 36% yield): ES-MS (m/z) 416 [M+H] + .
- the oil was taken into anhydrous acetontril ⁇ (150 mL) and phosphorous oxychlorid ⁇ (75 mL) was added to the solution.
- the mixture was brought to reflux under an atmosphere of nitrogen for 12 hours then cooled to room temperature and concentrated to an oil.
- the residue was taken into ethyl acetat ⁇ and th ⁇ solution cooled to 0°C followed by careful quenching by slow addition cf one volum ⁇ ⁇ quivalent of water.
- the organic layer was washed with additional water then with saturated aqueous sodium chloride. The organic layer was then concentrated to an oil and taken into dichloromethan ⁇ and methanol (1 :1 , 250 mL).
- the tide compound was prepared as described in Example 3.D, using 2-
- EXAMPLE 140 ER-SELECTIVITY IN U2OS OSTEOSARCOMA CELLS
- Human U2OS osteosarcoma cells were stably transfected with expression vectors for human full-length ER- ⁇ or ER- ⁇ , respectively, using standard molecular biology techniques. Stable subclones were generat ⁇ d that ⁇ xpr ⁇ ss ⁇ d high levels of ER- ⁇ or ER- ⁇ mRNA. The expression of ER- ⁇ and ER- ⁇ was confirmed using RNase protection analysis. The parental U2OS cells did not express any measurable amounts of eith ⁇ r ER- ⁇ or ER- ⁇ .
- Results of this assay are set forth in Table 4 for a number of representative compounds of this invention, as well as for the prior art test compounds.
- activity is expressed as IC 5 o calculated by 50% inhibition relativ ⁇ to DMSO control (100%).
- the prior art test compounds were 17- ⁇ - Estradiol, Raloxifene Hydrochloride, 4-Hydroxy-Tamoxifen, and the following compound disclosed in published PCT WO 96/21656 (referred to herein as "Compound A”):
- representative compounds of this invention showed specificity for ER- ⁇ over ER- ⁇ , while the prior art compounds (with the exception of 17- ⁇ -Estradiol) were selective for ER- ⁇ over ER- ⁇ .
- preferred components of this invention have an IC o of less than l ⁇ M, and more pref ⁇ rably 500nM or less.
- Tamoxifen resistant breast cancer cells in this case LCCl and LCC2 cells (R. Clarke, Georg ⁇ town University), were plated in 96-well dishes at 5000 cells per well in phenol-red free medium containing 5% charcoal-stripped serum. Thre ⁇ hours later, test compounds were prepared by serial dilution and added to the cells to yield a final concentration of 0.2%> DMSO. Compounds were prepared fresh and added daily for 4 days with media change after 48 hours. On the fifth day, [3H] -thymidine (2.5 ⁇ Ci/ml) was added to each well of the 96-well dish and the plate incubated at 37°C for 6 hours. At the end of the incubation, the cells were lysed and th ⁇ [3H]-thymidin ⁇ inco ⁇ orated determin ⁇ d using a scintillation counter.
Abstract
Compounds that modulate the estrogen receptor (ER) are disclosed, as well as pharmaceutical compositions containing the same. In a specific embodiment, the compounds are selective modulators for ER-β over ER-α. Methods are disclosed for modulating ER-β in cell and/or tissues expressing the same, including cells and/or tissue that preferentially express ER-β. More generally, methods for treating estrogen-related conditions are also disclosed, including conditions such as is breast cancer, testicular cancer, osteoporosis, endometriosis, cardiovascular disease, hypercholesterolemia, prostatic hypertrophy, prostatic carcinomas, obesity, hot flashes, skin effects, mood swings, memory loss, urinary incontinence, hairloss, cataracts, natural hormonal imbalances, and adverse reproductive effects associated with exposure to environmental chemicals.
Description
COMPOUNDS AND METHODS FOR MODULATION OF ESTROGEN RECEPTORS
TECHNICAL FIELD
This invention is generally directed to estrogen antagonists and agonists, including pharmaceutical compositions and uses thereof, and more specifically to compounds which selectively modulate estrogen receptor-beta (ER-β) activity.
BACKGROUND OF THE LNNENTION
The estrogen hormone has a broad spectrum of effects on tissues in both females and males. Many of these biological effects are positive, including maintenance of bone density, cardiovascular protection, central nervous system (CNS) function, and the protection of organ systems from the effects of aging. However, in addition to its positive effects, estrogen also is a potent growth factor in breast and endometrium that increases the risk of cancer.
Until recently, it has been assumed that estrogen binds to a single estrogen receptor (ER) in cells, causing conformational changes that result in release from heat shock proteins and binding of the receptor as a dimer to the so-called estrogen response element in the promoter region of a variety of genes. Further, pharmacologists have generally believed that non-steroidal small molecule ligands compete for binding of estrogen to ER, acting as either antagonists or agonists in each tissue where the estrogen receptor is expressed. Thus, such ligands have traditionally been classified as either pure antagonists or agonists. This is no longer believed to be correct.
Progress over the last few years has shown that ER associates with co- activators (e.g., SRC-1, CBP and SRA) and co-repressors (e.g., SMRT and N-CoR) that modulate the transcriptional activity of ER in a tissue-specific and ligand-specific manner. In addition, evidence now suggests that the majority of estrogen-regulated
genes do not have a classical estrogen response element. In such cases, ER interacts with the transcription factors critical for regulation of these genes. Transcription factors known to be modulated in their activity by ER include, for example, AP-1, NF-κB, C/EBP and Sp-1. Given the complexity of ER signaling, as well as the various types of tissue that express ER and its co-factors, it is now believed that ER ligands can no longer simply be classified as either pure antagonists or agonists. Therefore, the term "selective estrogen receptor modulator" (SERM) has been coined. SERMs bind to ER, but may act as an agonist or antagonist of estrogen in different tissues and on different genes. For example, two of the most well known drugs that behave as SERMs are Tamoxifen (Astra-Zeneca Pharmaceuticals) and Raloxifene (Eli Lilly & Co.). Studies with these two compounds, as well as other SERMs now in development, have demonstrated that the affinity of a SERM for its receptor in many cases does not correlate with its biological activity. Therefore, ligand-binding assays traditionally used in screening for novel ER modulators have not distinguished between tissue-selectivity and agonist/antagonist behavior.
In addition to Tamoxifen and Raloxifene, a number of other compounds have been disclosed to have estrogenic activity, such as those disclosed by Lednicer et al. (J. Med. Chem. 12, 881, 1969) and Bencze et al. (J. Med. Chem. 10, 138, 1967), as well as those disclosed in U.S. Patent Nos. 3,234,090, 3,277,106, and 3,274,213. Further, estrogen agonists/antagonists of the following structure are disclosed in published PCT WO 96/21656 to Cameron et al.:
More recently, a second estrogen receptor, ER-β, has been identified and cloned (Katzenellenbogen and Korach Endocrinology 138, 861-2 (1997); Kuiper et al,
Proc Natl. Acad. Sci. USA 93, 5925-5930, 1996; Mosselman et al., FEBS Lett. 392, 49-
53, 1996). ER-β, and the classical ER renamed ER-α, have significantly different amino acid sequences in the ligand binding domain and carboxy-terminal transactivation domains (-56% amino acid identity), and only 20% homology in their amino-terminal transactivation domain. This suggests that some ligands may have higher affinity to one receptor over the other. Further, ligand-dependent conformational changes of the two receptors, and interaction with co-factors, will result in very different biological actions of a single ligand. In other words, a ligand that acts as an agonist on ER-α may very well serve as an antagonist on ER-β. An example of such behavior has been described by Paech et al. (Science 277, 1508-1510, 1997). In that paper, estrogen is reported to activate an AP-1 site in the presence of ER-α, but to inhibit the same site in the presence of ER-β. In contrast, Raloxifene (Eli Lilly & Co.) and Tamoxifen and ICI- 182,780 (Zeneca Pharmaceuticals) stimulate the AP-1 site through ER-β, but inhibit this site in the presence of ER-α. Another example has been described by Sun et al. (Endocrinology 140, 800-4, 1999), wherein the R,R-enantiomer of a tetrahydrochrysene is reported to be an agonist on ER-α, but a complete antagonist on ER-β, while the S,S-enantiomer is an agonist on both receptors.
Furthermore, ER-α and ER-β have both overlapping and different tissue distributions, as analyzed predominantly by RT-PCR or in-situ hybridization due to a lack of good ER-β antibodies. Some of these results, however, are controversial, which may be attributable to the method used for measuring ER, the species analyzed (rat, mouse, human) and/or the differentiation state of isolated primary cells. Very often tissues express both ER-α and ER-β, but the receptors are localized in different cell types. In addition, some tissues (such as kidney) contain exclusively ER-α, while other tissues (such as uterus, pituitary and epidymis) show a great predominance of ER-α (Couse et al., Endocrinology 138, 4613-4621, 1997; Kuiper et al., Endocrinology 138, 863-870, 1997). In contrast, tissues expressing high levels of ER-β include prostate, testis, ovaries and certain areas of the brain (Brandenberger et al., J. Clin. Endocrinol Metab. 83, 1025-8, 1998; Enmark et al., J. Clinic. Endocrinol Metabol 82, 4258-4265, 1997; Laflamme et al., J. Neurobwl. 36, 357-78, 1998; Sar and Welsch, Endocrinology 140, 963-71, 1999; Shughrue et al., Endocrinology 138, 5649-52, 1997a; Shughrue et al., J. Comp. Neurol 388, 507-25, 1997b); Chang and Prins, The Prostate 40, 1 15-124, 1999.
The development of ER-α (Korach, Science 266, 1524-1527, 1994) and ER-β (Krege et al., Proc. Natl. Acad. Sci. USA 95, 15677-82. 1998) knockout mice further demonstrate that ER-β has different functions in different tissues. For example, ER-α knockout mice (male and female) are infertile, females do not display sexual receptivity and males do not have typical male-aggressive behavior (Cooke et al., Biol Reprod. 59, 470-5, 1998; Das et al., Proc. Natl. Acad. Sci. USA 94, 12786-12791, 1997; Korach, 1994; Ogawa et al., Proc. Natl. Acad. Sci. USA 94, 1476-81 , 1997; Rissman et al, Endocrinology 138, 507-10, 1997a; Rissman et al., Horm. Behav. 31, 232-243, 1997b). Further, the brains of these animals still respond to estrogen in a pattern that is similar to that of wild type animals (Shughrue et al., Proc. Natl. Acad. Sci. USA 94, 11008-12, 1997c), and estrogen still inhibits vascular injury caused by mechanical damage (Iafrati et al., Nature Med. 3, 545-8, 1997). In contrast, mice lacking the ER-β develop normally, are fertile and exhibit normal sexual behavior, but have fewer and smaller litters than wild-type mice (Krege et al., 1998), have normal breast development and lactate normally. The reduction in fertility is believed to be the result of reduced ovarian efficiency, and ER-β is the predominant form of ER in the ovary, being localized in the granulosa cells of maturing follicles. ER-β knockout mice display signs of prostatic hyperplasia with aging, which suggests that ER-β may normally protect against abnormal growth (Krege et al., 1998). ER-α/ER-β double knockout mice are viable, but infertile, and display a postnatal reversal of the ovaries (Couse et al., Science 286, 2328-2331 , 1999).
In summary, compounds which serve as estrogen antagonists or agonists have long been recognized for their significant pharmaceutical utility in the treatment of a wide variety of estrogen-related conditions, including conditions related to the brain, bone, cardiovascular system, skin, hair follicles, immune system, bladder and prostate (Barkhem et al., Mol. Pharmacol 54, 105-12, 1998; Farhat et al., FASEB J. 10, 615- 624, 1996; Gustafsson, Chem. Biol. 2, 508-1 1 , 1998; Sun et al., 1999; Tremblay et al., Endocrinology 139, 11 1-118, 1998; Turner et al., Endocrinology 139, 3712-20, 1998). In addition, a variety of breast and non-breast cancer cells have been described to express ER, and serve as the target tissue for specific estrogen antagonists (Brandenberger et al., 1998; Clinton and Hua, Crit. Rev. Oncol Hematol. 25, 1-9, 1997; Hata et al., Oncology 55 Suppl 1, 35-44, 1998; Rohlff et al., Prostate 37, 51-9, 1998;
Simpson et al, J Steroid Biochem Mol Biol 64, 137-45,1998; Yamashita et al., Oncology 55 Suppl 1, 17-22, 1998).
With the recent identification of the ER-β, and the recognition that ER-α and ER-β have different biological roles, ER-selective modulators would similarly possess significant clinical utility. Since ER-β is expressed strongly in a number of tissues including prostrate, bladder, ovary, testis, lung, small intestine, vascular endothelium, and various parts of the brain, compounds that selectively modulate ER-β would be of clinical importance in the treatment of a variety of diseases or conditions, such as prostate cancer, testicular cancer, cardiovascular diseases, neurodegenerative disorders, urinary incontinence, CNS, GI tract conditions, and bone and other cancers. Such compounds would have minimal effect on tissues that contains ER-α, and thus exhibit different side-effect profiles. For example, while estrogen replacement therapy is associated with a variety of beneficial effects (such as bone protection, cardiovascular effect, prevention of hot flashes, dementia, bone metabolism, etc.), such therapy also has adverse effects (such as breast and endometrial cancer, thrombosis, etc.). Some of these adverse effects .are believed to be mediated by ER-α or ER-β specific mechanisms. Thus, ER-β antagonists or agonists will display different therapeutic profiles compared to ER-α antagonists or agonists, and would be preferentially beneficial in tissues expressing high levels of ER-β (see, e.g., Nilsson et al., TEM 9, 387-395, 1998; Chang and Prins, The Prostate 40, 1 15-124, 1999). Furthermore, a number of investigators have shown that environmental chemicals and phytoestrogens preferentially interact with ER-β by triggering biological responses similar to that of estrogen (see, e.g., Kuiper et al., Endocrinology 139, 4252-4263, 1998). Thus, compounds that antagonize ER-β would also be important in regulating interactions with chemicals, affecting health, reproductive capacity and the like.
Accordingly, there is a need in the art for estrogen antagonists and agonists, including pharmaceutical compositions and methods relating to the use thereof. There is also a need for compounds that selectively modulate ER-β. The present invention fulfills these needs, and provides further related advantages.
SUMMARY OF THE INVENTION
In brief, the present invention is generally directed to estrogen antagonists and/or agonists, including pharmaceutical compositions containing the same, as well as to methods for treating estrogen-related conditions. Such conditions are more specifically discussed below, and generally include (but are not limited to) obesity, breast cancer, osteoporosis, endometriosis, cardiovascular disease, prostate cancer, menopausal syndromes, hair loss (alopecia), type-II diabetes, Alzheimer's disease, urinary incontinence, GI tract conditions, spermatogenesis, vascular protection after injury, endometriosis, learning and memory, CNS effects, plasma lipid levels, acne, cataracts, hirsutism, other solid cancers (such as colon, lung, ovarian, testis, melanoma, CNS, and renal), multiple myeloma, and lymphoma.
More specifically, the estrogen antagonists and/or agonists of this invention are compounds having the following structure (I):
(I) including stereoisomers and pharmaceutically acceptable salts thereof, wherein A, B, C, D, R), Ps.2, R3 and a are as identified in the following detailed description. In addition, pharmaceutical compositions are also disclosed containing one or more compounds of structure (I), in combination with a pharmaceutically acceptable carrier or diluent. In another embodiment, methods are disclosed for modulating cells and/or tissues that express ER-β by contacting the cell and/or tissue with an effective amount of a compound of structure (I). In an embodiment, the cell and/or tissue preferentially expresses ER-β over ER-α, such as cell and/or tissue of bone, bladder, uterus, ovary, prostate, testis, epididymis, gastrointestinal (GI) tract, kidney, breast, heart, vessel wall, immune system, lung, pituitary, hippocampus and hypothalamus.
In still a further embodiment, the present invention discloses methods for treating an estrogen-related condition by administering to an warm-blooded animal in need thereof an effective amount of a compound of structure (I) formulated as a pharmaceutical composition suitable for administration to the animal. In representative embodiments, the estrogen-related condition is breast cancer, osteoporosis, endometriosis, cardiovascular disease, hypercholesterolemia, prostatic hypertrophy, obesity, prostate cancer, menopausal syndromes, type-II diabetes, Alzheimer's disease, urinary incontinence, GI tract conditions, spermatogenesis, vascular protection after injury, endometriosis, learning and memory, CNS effects, plasma lipid levels, acne, hirsutism, other solid cancers (such as colon, lung, ovarian, testis, melanoma, CNS, and renal), multiple myeloma, lymphoma, prostatic carcinomas, obesity, hot flashes, skin effects, mood swings, memory loss, and/or adverse reproductive effects associated with exposure to environmental chemicals. In other embodiments, methods are disclosed for inhibiting a cyctokine, such as IL-6 and GM-CSF, in an animal in need thereof, as well as methods for treating cancer associated therewith.
These and other aspects of this invention will be evident upon reference to the attached drawings and the following detailed description. To that end, certain references are cited herein each of which are hereby incorporated by reference in their entirety.
BRIEF DESCRIPTION OF THE DRAWINGS
Figures 1A and IB illustrate proliferation of Tamoxifen resistant LCC1 and LCC2 breast cancer cell lines when exposed to a representative compound of this invention.
DETAILED DESCRIPTION OF THE INVENTION As mentioned above, the present invention is directed to compounds that have activity as estrogen antagonists and/or agonists, as well as pharmaceutical compositions containing one or more of such compounds and methods related to the same. As estrogen antagonists and/or agonists, the compounds of this invention have utility in the treatment of a wide range of estrogen-related conditions. In this context, the term "treatment" includes both treatment and/or prevention of an estrogen-related
condition. Thus, the compounds of this invention may be administered as a therapeutic and/or prophylactic agent. An estrogen "agonist" is a compound that binds to ER and mimics the action of estrogen in one or more tissues, while an "antagonist" binds to ER and blocks the action of estrogen in one or more tissues. Further, the term "estrogen- related condition" encompasses any condition associated with elevated or depressed levels of estrogen, a selective estrogen receptor modulators (SERM), ER-α or ER-β.
Accordingly, the compounds of the present invention may also be used within a method for treating estrogen-related conditions, including (but not limited to) breast cancer, osteoporosis, . endometriosis, cardiovascular disease, hypercholesterolemia, prostatic hypertrophy, prostatic carcinomas, obesity, hot flashes, skin effects, mood swings, memory loss, menopausal syndromes, hair loss (alopecia), type-II diabetes, Alzheimer's disease, urinary incontinence, GI tract conditions, spermatogenesis, vascular protection after injury, endometriosis, learning and memory, CNS effects, plasma lipid levels, acne, hirsutism, other solid cancers (such as colon, lung, ovarian, testi, melanoma, CNS, and renal), multiple myeloma, cataracts, lymphoma, and adverse reproductive effects associated with exposure to environmental chemicals.
In one aspect of this invention, it has been found that the compounds of this invention are selective estrogen receptor modulators and, more specifically, are selective to ER-β. Accordingly, in this aspect of the invention, the compounds have utility as agents for treatment of osteoporosis, hormonally regulated cancer, combination treatment of cancer (such as with taxol cisplatin or chemotherapy), women's gynecologic health issues, and health conditions resulting from exposure to environmental chemicals. The compounds of this invention have the following structure (I):
(I)
including stereoisomers and pharmaceutically acceptable salts thereof; wherein a is 0, 1 or 2;
A, B and C are independently CH, CR or N; D is -(CH2)-- or -(CH2)nC(=O)(CH2)m-;
Ri represents one or two substituents independently selected from -X-Y;
R is Cι-8alkyl, Cό-i-iaryl, C7-i2aralkyl, -C(=O)R5, a five- or six- membered heterocycle or heterocyclealkyl containing up to two heteroatoms selected from O, NRς and S(O)9, or a bicyclic ring system contain a five- or six-membered heterocycle fused to phenyl, wherein each of the above groups are optionally substituted with one to three substituents independently selected from -X-Y or R-,; and
R3 is hydrogen, -R*,
-(CH2),C(=O)NR6R7, -(CH:),C(=O)NR6(CH2)nC(=O)R7R8,
-(CH2),OR6, -(CH2)JSO£R6 or -(CH2)JSO2NR6R7; and wherein
R is at each occurrence independently halogen, hydroxy, carboxy, Cι-6alkyl,
Cι-4thio,
Cι- alkylsulfonyl, (hydroxy)Cι-4alkyl, C6-i2aryl, C7_12ara!kyl, -C(=O)OH, -C(=O)OR, -OC(=O)R, -C(=O)NHR, -C(=O)NRR, -C(=O)NHOR, -SO2NHR, -NHSO2R, -CN, -NO2, -NH2, CMalkylamino, CMdialkylamino, -NHC(=O)R,
or six-membered heterocycle), a five- or six-membered heterocycle, or a five- or six-membered heterocycle fused to phenyl;
R5, Rs, R and R8 are at each occurrence independently hydrogen,
C].8alkyl, C6-ι2aryl. C7-ι2aralkyl, or a five- or six-membered heterocycle or heterocyclealkyl containing up to two heteroatoms selected from O, NRc and S(O)g, wherein each of the above
groups are optionally substituted with one to three substituents independently selected from R-i; X is at each occurrence independently a direct bond; - CH2)nZ(CH2)m-;
-O(CH2)nZ(CH2)m-;
-S(CH2)nZ(CH2)m-;
-NRc(CH2)nZ(CH2)m-;
-O(CH2)nCRaRb-; -NRc(CH2)nCRaRb-;
-OCHReCHRd-; or
-SCHRcCHRj-; Y is at each occurrence independently halogen; -Re;
-NReRf,
Z is CH2, CH=CH, C≡C, O, NRc, S(O)q, C(=O), C(OH)Rc, C(-O)NRc,NRcC(=O), C(=O)NRc, NRcC(=O) or ~" ;
G is O, S or NRe; n and m are at each occurrence independently 0, 1, 2 or 3; p is at each occurrence independently 1, 2 or 3; q is at each occurrence independently 0, 1 or 2; r is at each occurrence independently 1, 2, 3, 4 or 5; s is at each occurrence independently 0, 1, 2, 3 or 4; R is at each occurrence independently Cι-6alkyl;
Ra and RD .are at each occurrence independently Cι-8alkyl or taken together form a C3- cyclic alkyl;
Re and Rj are at each occurrence independently hydrogen or Cι.4alkyl; and Re and Rf are at each occurrence independently hydrogen, C6-i2aryl,
Cι.8alkyl, C -i2aralkyl, a five- or six-membered heterocycle, or a five- or six-membered heterocycle fused to phenyl; or wherein Re or Rf form a 3-8 membered nitrogen-containing heterocyclic alkyl with Ra or Rb; and wherein each Re and R are optionally substituted with up to three substituents independently selected
As used herein, the above terms have the following meaning:
"Halogen" means F, CI, Br and I. "C,.4alkyl", "C,.6alkyl" and "Cι-8alkyl" means a straight chain or branched, cyclic or non-cyclic, saturated or unsaturated carbon chain having from 1 to 4, 6 or 8 carbon atoms, respectively. In one embodiment, the Cι-χ alkyl (where X is 4, 6 or 8 as disclosed above) is a fully saturated, straight chain alkyl such as methyl, ethyl, n-propyl, n-butyl, n-pentyl, n-hexyl and the like. In another embodiment, the C].\ alkyl
is a fully saturated cyclic alkyl such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and the like, or an alkyl(cycloalkyl) moiety such .as methylenecyclopropyl, methylenecyclobutyl, methylenecyclopentyl, methylenecyclohexyl, and the like, or an unsaturated cyclic alkyl. In still a further embodiment, the Cι-X alkyl is a fully saturated, branched alkyl such as iso-propyl, iso-butyl, tert-butyl, iso-pentyl, iso-hexyl, and the like. In yet another embodiment, the -x alkyl is an unsaturated straight chain alkyl such as ethylenyl, propylenyl, 1-butenyl, 1-pentenyl, 1-hexenyl, and the like.
"C6-ι2aryl" means a carbocyclic aromatic moiety containing from 6 to 12 carbon atoms. In one embodiment, the C6-i2aryl is phenyl, tetralinyl or napthalenyl, and typically is phenyl.
"C -i2aralkyl" means an arene containing from 7 to 12 carbon atoms, and has both aliphatic and aromatic components. In one embodiment, the C7.12 aralkyl is benzyl, ethylenephenyl, propylenephenyl, and the like.
"Five- or six-membered heterocycle" means a heterocyclic ring containing up to two heteroatoms selected from O, NRc and S(O)?, and wherein the number of carbon and heteroatoms of the ring total 5 or 6, including both saturated and unsaturated, aromatic and non-aromatic ring systems, such as pyridinyl, pyrimidinyl, furanyl, thienyl, triazenyl, imidazolyl, thiazolyl, pyrazolyl, pyridazinyl, pyrazinyl, and the like. "Five- or six-membered heterocyclealkyl" means a Cι-6alkyl having at least one hydrogen replaced with a five- or six-membered heterocyle, such as -CH (hererocycle), and the like.
"Ci-.talkoxy" means a -O(Cι- alkyl), where x is 4, 6 or 8.
"C acyloxy" means -OC(=O)C alkyl. "Cι--tthio" means -SCι- alkyl.
"Ci- alkylsulfinyl" means -SOCι- alkyl.
"Cι_ιalkylsulfonyl" means • Sθ2Cι- alkyl.
"(hydroxy)Cj-4alkyl" means Cι--,alkyl wherein a hydrogen atom has been substituted by hydroxyl. "C|_,alkylamino" means -NHC,-4alkyl.
"Cι--dialkylammo" means -N(Cι- alkyl)( Cι- alkyl).
"Cι-thaloalkyl" means a Cι_ alkyl having at least one hydrogen replaced with halogen, such as trifluoromethyl and the like.
In one aspect of structure (I), A and B are both CH, C is N, D is -CH2-, and the compounds of this invention have the following structure (IJa) when a is 1, (Lib) when a is 0, and (lie) when a is 2:
(Ha) (lib) (lie)
In other aspects of this invention, the compounds of structure (I) have the following structures (III), (IV), (V) or (VI):
(III) (IN)
(V) (NI)
In one embodiment of structure (Ha), R2 is phenyl optionally substituted with one, two or three substituents independently selected from R4, R3 is hydrogen, and the compounds of this invention have the following structure (IIa-1):
(IIa-1)
In another embodiment of structure (Ha), R2 is pyridinyl optionally substituted with one, two or three substituents independently selected from R-t, R3 is hydrogen, and the compounds of this invention have the following structures (IIa-2) or (IIa-3):
(IIa-2) (IIa-3)
In another embodiment of structure (Ila), Ri is
a the 4-position, R3 is hydrogen, and the compounds of this invention have the following structure (IIa-4):
In yet further embodiments, the compounds of this invention have the following structure (IIa-5) or (IIa-6):
(IIa-5) (IIa-6)
In still further embodiments, the compounds of this invention have the following structure (IIa-7):
(IIa-7) In another embodiment, compounds of this invention have the following structure (Nil):
(VII) For purpose of illustration, representative compounds of structure (Nil) are set forth in the Table 1.
Table 1 Representative Compounds of Structure (NLT)
In still a further embodiment, D of structure (I) is carbonyl - that is, -(CH2)„C(=O)(CH2)m- wherein both n and m are zero - and the compounds of this invention have the following structure (VIII):
In one aspect of this embodiment, R3 is hydrogen and compounds of this invention have the following structure (Villa):
(Villa)
For purposes of illustration, representative compounds of structure (Villa) are set forth in Table 2.
Table 2 Representative Compounds of Structure (Villa)
In one aspect of this embodiment, R3 is hydrogen and compounds of this invention have the following structure (IXa):
(IXa)
For purposes of illustration, representative compounds of structure (IXa) are set forth in Table 3.
Table 3 Representative Compounds of Structure (IXa)
As noted above, compounds of this invention have structure (I), wherein a is 1, 2 or 3, yielding a fused, bicyclic six-five-, six-six- or six-seven-membered ring system. In a typical embodiment, a is 1.
With regard to the A and B moieties, in a typical embodiment both A and B are CH, yielding a benzene ring substituted with the Ri moiety. Other representative groups in this regard include those embodiments wherein either A or B is nitrogen, or wherein both A and B are nitrogen. Representative C moieties include both nitrogen and CH. In a typical embodiment, the C moiety is nitrogen.
D moieties of this invention include -(CH2 - and -(CH )„C(=O)(CH )w-. When D is -(CH2)r-, r is typically 1 or 2, and more typically 1 - such that D moiety is methylene. In the embodiment wherein D is -(CH2)ΛC(=O)(CH2)OT-, n and m are typically 0, 1 or 2. In one embodiment, both n and m are zero, and D is carbonyl.
Ri groups of this invention have the formula -X-Y. As used herein, Ri designates either one or two Ri substuents. In the case of two Rj substituents, each of the Ri substituents may be the same or different. Typically. Ri refers to a single substituent as represented by -X-Y. In one embodiment, X is -(CH2)„Z(CH2)m- and Y has the following structure:
Representative R\ groups in this regard include those wherein n is zero and Z is oxygen, and having the following structure:
For example, when W is oxygen, p and q are both 1 , representative Ri groups include the following (wherein m is, for example, 2 or 3):
Representative R\ groups also include those having the following structure:
Representative R2 groups include substituted or unsubstitued C6-i2aryl, and typically substituted phenyl. In one embodiment, R2 is phenyl substituted with one or two substituents selected from halogen, such as fluorine. Again, further representative R2 groups include those as set forth below in Examples 1-139.
10 Representative R3 groups include hydrogen and Cι-4alkyl, and R3 is typically hydrogen or methyl.
The compounds of this invention may be made by the procedures and tecliniques disclosed in the Examples, as well as by known organic synthesis techniques, including the techniques disclosed in published PCT WO 96/21656 (which i D reference is incoφorated herein in its entirety) but utilizing the corresponding benzyl starting materials rather than the phenyl compounds. For example, the compounds of this invention may be made by the following general reaction schemes.
Reaction Scheme 1 :
IJAIH4 0
(I) (R = H) (I) (C = N)
In the above Reaction Scheme 1, aryl acid chloride (a), on treatment with primary amine (b) affords aryl secondary amide (c), which is reduced with lithium aluminum hydride in ethereal solvents to yield secondary amine (d). Subsequent acylation of (d) with acid chloride (e) leads to tertiary amide (f), which is cyclized in hot phosphorus oxychloride to yield dihydroisoquinolinium salt (g). Reduction of (g) with sodium borohydride yields compounds of structure (I) where C is N, which upon demethylation with boron tribromide in methylene chloride affords compounds of structure (I) where R3 is hydrogen.
Reaction Scheme 2:
In Reaction Scheme 2, tertiary amide (f) as prepared in Reaction Scheme
1 is cyclized upon heating in phosphorous oxychloride. The cyclized product - that is, the imine salt (g) or the enamine (h) - is R2 dependent. Reduction of (g) with sodium borohydride or reduction of (h) with hydrogen and palladium on carbon affords compounds of structure (I).
Reaction Scheme 3:
In Reaction Scheme 3, debenzylation of (i) using hydrogen and palladium on carbon provides the hydroxybenzyltetrahydroisoquinoline (j). Alkylation with 2-chloroethyl-peperidinehydrochloride using potassium carbonate yields (1), which is the demethylated using boron tribromide to provide compounds of structure (II).
Reaction Scheme 4:
The above Reaction Scheme 4 illustrates the synthesis of compounds of structure (I) wherein C is CH. In this scheme, tetralone (m) is deprotonated with a base, such as LDA, and alkylated with a benzylbromide (n) - or a corresponding heterocylic compound when A and B are other than CH - to yield the adducf (p). Treatment of (p) with mesylchloride and triethylamine followed by treatment with hydrogen and palladium hydroxide (or palladium on carbon) affords compounds of structure (I) wherein C is CH.
Reaction Scheme 5:
(u) (t)
H2, Pd(OH)2
(I) (C = CH)
(w)
In Reaction Scheme 5, compounds of structure (I) where C is CH may be made according to the above reaction scheme. Alkyloxy tetralone (q) is deprotonated with a base, such as LDA, and alkylated with a benzylbromide (r) to yield the benzyl adduct (s). Treatment of (s) with an organohthium provides the hydroxy intermediate (t), which is then reacted with mesylchloride and triethylamine to afford the dehydrated product (u). Reduction and debenzylation of (u) using hydrogen and palladium hydroxide on carbon affords (v). Subsequent alkylation using 2-chloroethylpiperidine hydrochloride and base yields compounds of structure (I) where C = CH, which can be converted to the corresponding hydroxyl (w) by dealkylation using boron tribromide. (w)
Reaction Scheme 6:
In Reaction Scheme 6, compounds of structure (I) where D is carbonyl may be made according to the above reaction scheme. Ketone (x) is oxidized with selenium dioxide to yield the glyoxal (y). Treatment of (y) with secondary amine (z) and trifluoroacetic acid provides compounds of structure (I) wherein D is carbonyl, which can be converted to the corresponding hydroxyl (aa) by dεbenzylation using hydrogen and palladium on carbon.
Reaction Scheme 7:
(b) R2NH2 AcOH
The above Reaction Scheme 7 illustrates the synthesis of compounds of structure (I) wherein a is 0. The dihydroisobenzofuran (bb) is prepared as described by Sakamoto et al. (Chem. Pharm. Bull. 31, 2698-2707, 1983). Treatment of (bb) with aldehyde (cc) provides the adduct (dd), which upon reaction with primary amine (b) yields the isoindolinone (ee). The double bond of (ee) is reduced using hydrogen and palladium on carbon to yield the corresponding isoindolinone (ff). Subsequent reduction of the carbonyl of (ff) with borane provides compounds of structure (I) where
a = 0, which can be converted to the corresponding hydroxyl (gg) upon treatment with boron tribromide.
One of ordinary skill in this field will recognize that certain compounds of this invention will contain atoms which may be in a particular optical or geometric configuration. Likewise, one will recognize that various pharmaceutically acceptable esters and salts may be prepared from certain compounds of this invention. All of such stereoisomers, esters and salts are included in this invention.
The methods for treating estrogen-related conditions of this invention - such as breast cancer, osteoporosis, endometriosis, cardiovascular disease, hypercholesterolemia, prostatic hypertrophy, prostate cancer, obesity, hot flashes, skin effects, mood swings, memory loss, menopausal syndromes, type-II diabetes, Alzheimer's disease, urinary incontinence, GI tract conditions, spermatogenesis, vascular protection after injury, endometriosis, learning and memory, CNS effects, plasma lipid levels, acne, hirsutism, other solid cancers (such as colon, lung, ovarian, testis, melanoma, CNS, and renal), multiple myeloma, lymphoma, and adverse reproductive effects associated with exposure to environmental chemicals - include administration of an effective amount of a compound of structure (I), or a salt or ester thereof, as the active ingredient. Pharmaceutically acceptable salts of the compounds of structure (I) are typically salts of non-toxic type commonly used, such as salts with organic acids (e.g., formic, acetic, trifluoroacetic, citric, maleic, tartaric, methanesulfonic, benzenesulfonic or toluenesulfonic acids), inorganic acids (e.g., hydrochloric, hydrobromic, sulfuric or phosphoric acids), and amino acids (e.g., aspartic or glutamic acids). These salts may be prepared by the methods known to chemists of ordinary skill. The compounds of this invention may be administered to animals
(including humans) orally or parenterally in the conventional form of preparations, such as capsules, microcapsules, tablets, granules, powder, troches, pills, suppositories, injections, suspensions and syrups. Suitable formulations may be prepared by methods commonly employed using conventional, organic or inorganic additives, such as an excipient (e.g., sucrose, starch, mannitol, sorbitol, lactose, glucose, cellulose, talc, calcium phosphate or calcium carbonate), a binder (e.g., cellulose, methylcellulose, hydroxymethylcellulose, polypropylpyrrolidone, polyvinylprrolidone, gelatin, gum
arabic, polyethyleneglycol, sucrose or starch), a disintegrator (e.g., starch, carboxymethylcellulose, hydroxypropylstarch, low substituted hydroxypropylcellulose, sodium bicarbonate, calcium phosphate or calcium citrate), a lubricant (e.g., magnesium stearate, light anhydrous silicic acid, talc or sodium lauryl sulfate), a flavoring agent (e.g., citric acid, menthol, glycine or orange powder), a preservative (e.g., sodium benzoate, sodium bisulfite, methylparaben or propylparaben), a stabilizer (e.g., citric acid, sodium citrate or acetic acid), a suspending agent (e.g., methylcellulose, polyvinyl pyrroliclone or aluminum stearate), a dispersing agent (e.g., hydroxypropylmethylcellulose), a diluent (e.g., water), and base wax (e.g., cocoa butter, white petrolatum or polyethylene glycol). The amount of the active ingredient in the medical composition may be at a level that will exercise the desired therapeutical effect; for example, about 0.1 mg to 100 mg in unit dosage for both oral and parenteral administration.
The active ingredient may be usually administered one to four times a day with a unit dosage of 0.1 mg to 100 or 200 mg in human patients, but the above dosage may be properly varied depending on the age, body weight and medical condition of the patient and the type of administration. A preferred dose is 0.25 mg to about 60 mg in human patients. One dose per day is preferred.
The compounds of this invention have utility as estrogen agonists and antagonists, as well as pharmaceutical agents or intermediates thereto. Those which are estrogen agonists are useful for oral contraception; relief for the symptoms of menopause; prevention of threatened or habitual abortion; relief of dysmenorrhea; relief of dysfunctional uterine bleeding; relief of endometriosis; an aid in ovarian development; treatment of acne; diminution of excessive growth of body hair in women (hirsutism); the prevention and treatment of cardiovascular disease; prevention and treatment of atherosclerosis; prevention and treatment of osteoporosis; treatment of benign prostatic hypeφlasia and prostatic carcinoma obesity; and suppression of post- parturn lactation. These agents also have a beneficial effect on plasma lipid levels and as such are useful in treating and preventing hypercholesterolemia. Those which are estrogen antagonists are useful as antiestrogens in, for example, breast and ovarian tissue and thus are useful in the treatment and prevention of breast and ovarian cancer.
Pharmaceutical chemists will easily recognize that physiologically active compounds which have accessible hydroxy groups are frequently administered in the form of pharmaceutically acceptable esters. The literature concerning such compounds, such as estradiol, provides a great number of instances of such esters. The compounds of this invention are no exception in this respect, and can be effectively administered as an ester, formed on the hydroxy groups, just as one skilled in pharmaceutical chemistry would expect. It is believed that esters are metabolically cleaved in the body, and that the actual drug, which such form is administered, is the hydroxy compound itself. It is possible, as has long been known in pharmaceutical chemistry, to adjust the rate or duration of action of the compound by appropriate choices of ester groups.
The pharmaceutically acceptable acid addition salts of the compounds of this invention may be formed of the compound itself, or of any of its esters, and include the pharmaceutically acceptable salts which are often used in pharmaceutical chemistry. For example, salts may be formed with inorganic or organic acids such as hydrochloric acid, hydrobromic acid, hydroiodic acid, sulfonic acids including such agents as naphthalenesulfonic, methanesulfonic and toluenesulfonic acids, sulfuric acid, nitric acid, phosphoric acid, tartaric acid, pyrosulfuric acid, metaphosphoric acid, succinic acid, formic acid, phthalic acid, lactic acid and the like, most preferable with hydrochloric acid, citric acid, benzoic acid, maleic acid, trifluoroacetate salt, acetic acid and propionic acid. It is usually preferred to administer a compound of this invention in the form of an acid addition salt, as it is customary in the administration of pharmaceuticals bearing a basic group such as the pyrrolidino ring.
The compounds of this invention, as discussed above, are very often administered in the form of acid addition salts. The salts are conveniently formed, as is usual in organic chemistry, by reacting the compound of this invention with a suitable acid, such as have been described above. The salts are quickly formed in high yields at moderate temperatures, and often are prepared by merely isolating the compound from a suitable acidic wash in the final step of the synthesis. The salt-forming acid is dissolved in an appropriate organic solvent, or aqueous organic solvent, such as an alkanol, ketone or ester. On the other hand, if the compound of this invention is desired in the free base form, it is isolated from a basic final wash step, according to the usual practice. A typical technique for preparing hydrochlorides is to dissolve the free base in a suitable
solvent and dry the solution thoroughly, as over molecular sieves, before bubbling hydrogen chloride gas through it.
The dose of a compound of this invention to be administered to a human is rather widely variable and subject to the judgment of the attending physician. It should be noted that it may be necessary to adjust the dose of a compound when it is administered in the form of a salt, such as a laureate, the salt forming moiety of which has an appreciable molecular weight. The general range of effective administration rates of the compounds is from about 0.05 mg/day to about 200 mg/day. A preferred rate range is from about 0.25 mg/day to 60 mg/day. Of course, it is often practical to administer the daily dose of compound in portions, at various hours of the day. However, in any given case, the amount of compound administered will depend on such factors as the solubility of the active component, the formulation used and the route of administration.
The route of administration of the compounds of this invention is not critical. The compounds are known to be absorbed from the alimentary tract, and so it is usually preferred to administer a compound orally for reasons of convenience. However, the compounds may equally effectively be administered percutaneously, or as suppositories for absoφtion by the rectum, if desired in a given instance.
The compounds of this invention are usually administered as pharmaceutical compositions which are important and novel embodiments of the invention because of the presence of the compounds. All of the usual types of compositions may be used, including tablets, chewable tablets, capsules, solutions, parenteral solutions, troches, suppositories and suspensions. Compositions are formulated to contain a daily dose, or a convenient fraction of daily dose, in a dosage unit, which may be a single tablet or capsule or convenient volume of a liquid.
Any of the compounds may be readily formulated as tablets, capsules and the like; it is preferable to prepare solutions from water-soluble salts, such as the hydrochloride salt. In general, all of the compositions are prepared according to methods usual in pharmaceutical chemistry. Capsules are prepared by mixing the compound with a suitable diluent and filling the proper amount of the mixture in capsules. The usual diluents include inert powdered substances such as starch of many different kinds, powdered cellulose, especially crystalline and microcrystalline
cellulose, sugars such as fructose, mannitol and sucrose, grain flours and similar edible powders.
Tablets are prepared by direct compression, by wet granulation, or by dry granulation. Their formulations usually incoφorate diluents, binders, lubricants and disintegrators as well as the compound. Typical diluents include, for example, various types of starch, lactose, mannitol, kaolin, calcium phosphate or sulfate, inorganic salts such as sodium chloride and powdered sugar. Powdered cellulose derivatives are also useful. Typical tablet binders are substances such as starch, gelatin and sugars such as lactose, fructose, glucose and the like. Natural and synthetic gums are also convenient, including acacia, alginates, methylcellulose, polyvinylpyrrolidine and the like. Polyethylene glycol, ethylcellulose and waxes can also serve as binders.
A lubricant is typically necessary in a tablet formulation to prevent the tablet and punches from sticking in the die. The lubricant is chosen from such slippery solids as talc, magnesium and calcium stearate, stearic acid and hydrogenated vegetable oils. Tablet disintegrators are substances which swell when- wetted to break up the tablet and release the compound. They include starches, clays, celluloses, algins and gums. More particularly, corn and potato starches, methylcellulose, agar, bentonite, wood cellulose, powdered natural sponge, cation-exchange resins, alginic acid, guar gum, citrus pulp and carboxymethyl cellulose, for example, may be used as well as sodium lauryl sulfate. Tablets are often coated with sugar as a flavor and sealant, or with film-forming protecting agents to modify the dissolution properties of the tablet. The compounds may also be formulated as chewable tablets, by using large amounts of pleasant-tasting substances such as mannitol in the formulation, as is now well - established in the art. When it is desired to administer a compound as a suppository, the typical bases may be used. Cocoa butter is a traditional suppository base, which may be modified by addition of waxes to raise its melting point slightly. Water-miscible suppository bases comprising, particularly, polyethylene glycols of various molecular weights are in wide use. The effect of the compounds may be delayed or prolonged by proper formulation. For example, a slowly soluble pellet of the compound may be prepared and incoφorated in a tablet or capsule. The technique may be improved by making
pellets of several different dissolution rates and filling capsules with a mixture of the pellets. Tablets or capsules may be coated with a film which resists dissolution for a predictable period of time. Even the parenteral preparations may be made long-acting, by dissolving or suspending the compound in oily or emulsified vehicles which allow it to disperse only slowly in the serum.
The following examples are offered by way of illustration, not limitation.
EXAMPLES
EXAMPLE 1
SYNTHESIS OF 1 -(4-BROMOBENZYL)-6-METHOXY-2-PHENYL-
1 ,2,3,4-TETRAHYDROISOQUTNOLINE
A. 2-(3-Methoxyphenyl)-N-phenylacetarnide
To a solution of 3-methoxyphenylacetyi chloride (2.3 g, 12.5 mmol) in ethyl acetate (30 mL) was added a solution of aniline (1.16 g, 12.5 mmol) in ethyl acetate (30 mL). After 3 hours, the reaction was poured into water (50 mL). The organic layer was separated, dried over MgSO , filtered and concentrated to provide the title compound (2.67 g, 89% yield): EI-MS (m/z) 241.
B. {2-(3-Methoxyphenyl)ethyl}phenylamine
To a solution of 2-(3-methoxyphenyl)-N-phenylacetamide (2.0 g, 8.3 mmol) in anhydrous tetrahydrofuran (30 mL) under nitrogen was added lithium aluminum hydride (1.59 g, 42 mmol) in small portions over a 1 hour period. After 16 hours, the reaction was poured over ice and the crude product extracted with ethyl acetate (2 x 100 mL). The organic layer was dried ov er MgSO , filtered and concentrated to provide the title compound (1.3 g, 69% yield): EI-MS (m z) 227. C. 2-(4-Bromophenyl)-N- {2-(3-methoxyphenyl)ethyl}-N-phenylacetamide
To a solution of {2-(3-methoxyphenyl)ethyl}phenylamine (1.06 g, 4.65 mmol) in ethyl acetate (80 mL) under nitrogen was added a solution of 4- bromophenylacetyl chloride (1.06 g, 4.65 mmol) in ethyl acetate (20 mL), the
bromophenylacetyl chloride being prepared from the corresponding carboxylic acid (1 g, 4.65 mmol) and oxalyl chloride (0.61 mL, 6.98 mmol) in CH2C12 (20 mL). After 1 hour, the reaction was poured into water (50 mL). The organic layer was dried over MgSO4, filtered and concentrated to provide the title compound (1.92 g, 98% yield): EI- MS (m/z) 423.
D. 1 -(4-Bromobenzyl)-6-methoxy-2-phenyl- 1 ,2,3 ,4-tetrahydroisoquinoIine A solution of 2-(4-bromophenyl)-N-{2-(3-methoxyphenyl)ethyl}-N- phenylacetamide (1.0 g, 2.4 mmol) in phosphorous oxychloride (10 mL) under nitrogen was heated to 80°C. After 15 hours, the reaction was cooled to RT and slowly poured over ice. Potassium iodide (0.78 g, 4.7 mmol) was then added to the mixture, and after 30 minutes, the quinolinium salt was extracted with ethyl acetate (2 X 100 mL). The organic layer was dried over MgSO4, filtered and concentrated. The residue was then dissolved in methanol (25 mL), and sodium borohydride (0.27 g, 7.2 mmol) was slowly added. After 30 minutes, the reaction was concentrated and partitioned between ethyl acetate and water. The organic layer was dried over MgSO4. filtered and concentrated to provide the title compound (0.20 g, 21% yield): Η NMR (CDC13) 6.6-7.4 (m, 12H), 4.82 (t, 1H), 3.60 (s, 3H), 3.58 (m, 2H), 2.6-3.2 (m 4H); EI-MS (m/z) 407.
EXAMPLE 2 SYNTHESIS OF 1 -(4-BROMOBENZYL)-2-PHENYL- 1 ,2,3,4-TETRAHYDR0IS0QUIN0LIN-6-0L
To a solution of l-(4-bromobenzyl)-6-methoxy-2-phenyl-l,2,3,4- tetrahydroisoquinoline (0.10 g, 0.25 mmol) in CH2CI2 (15 mL) at 0°C under nitrogen was added boron tribromide (1.47 mL, 1.47 mmol). The reaction was allowed to reach RT. After 8 hours, the reaction was poured into water (10 mL) and neutralized with
saturated sodium bicarbonate. Additional CH2CI2 (25 mL) was added, the organic layer was separated, dried over MgSO4, filtered and concentrated. The residue was then chromatographed (SiO2, 2: 1, hexanes/ethyl acetate) to provide the title compound (0.010 g, 10% yield): 1H NMR (CDC13) 7.33 (d, 2H), 7.24 (dd, 2H), 6.97 (d, 1H), 6.88 (d, 2H), 6.80 (d, 2H), 6.75 (dd, 2H), 6.66 (m, 1H), 6.27 (s, 1H), 4.78 (t, 1H), 3.53 (m 2H), 3.13 (dd, 1H), 2.96 (m, 2H), 2.62 (m, 1H); ES-MS (m/z) 392 [M-H]" .
EXAMPLE 3
SYNTHESIS OF 2-PHENYL-1 - {4-[(2-?IPERIDYL)ETHOXY]BENZYL}-
L ,2,3,4-TETRAHYDR0IS0QUIN0LIN-6-0L
A. N-{2-(3-Methoxyphenyl)ethyl}-N-phenyl-2-{4-(phenylmethoxy)phenyl} acetamide
The title compound was prepared as described in Example l.C, using 4- benzyloxyphenylacetyl chloride (2.28 g, 8.27 mmol) prepared from the corresponding carboxylic acid (2.0 g. 8.27 mmol) and oxalyl chloride (5.25 mL, 41.4 mmol) in CH2CI2 (50 mL) (3.36 g, 90% yield): ES-MS (m/z) 452 [M+H]+.
B. 1 - {4-(/Phenylmethoxy)benzyll -6-methoxy-2-phenyl- 1 ,2,3,4- tetrahydroisoquinoline
The title compound was prepared as described in Example 1.D, using N- {2-(3-methoxyphenyl)ethyl}-N-phenyl-2-{4-(phenylmethoxy)phenyl} acetamide (0.5 g,
1.11 mmol) to afford the title compound (0.19 g, 39% yield): ES-MS (m/z) 436
[M+H]+.
C. 1 -(4-Hydroxybenzyl)-6-methoxy-2-phenyl- 1.2.3.4-tetrahydroisoquinoline
A solution of l- {4-(phenylmethoxy)benzyl}-6-methoxy-2-phenyl- 1,2,3,4-tetrahydroisoquinoline (0.60 g, 1.38 mmol), palladium (5% wt. on activated
carbon, 0.06 g), and glacial acetic acid (3 drops) in ethanol (30 mL) was stirred under hydrogen for 15 hours. The reaction was filtered and concentrated to provide the title compound (0.30 g, 63% yield): ES-MS (m/z) 346 [M+H]+.
D. 6-Methoxy-2-phenyl- 1 - {4- (2-piperidyl)ethoxy]benzyl} - 1 ,2,3,4- tetrahydroisoquinoline
A solution of l-(4-hydroxybenzyl)-6-methoxy-2-phenyl- 1,2,3,4- tetrahydroisoquinoline (0.30 g, 0.87 mmol), 2-chloroethylpiperidine hydrochloride
(0.32 g, 1.74 mmol) and potassium carbonate (0.24 g, 1.74 mmol) in dimethyl formamide (15 mL) was heated to 80°C. After 6 hours, the mixture was cooled to RT, poured into water (30 mL), and neutralized using a saturated solution of ammonium chloride. The product was extracted with ethyl acetate (2 X 75 mL), dried over MgSO , filtered and concentrated. The residue was then chromatographed (SiO2, 10:1 ethyl acetate/ethanol) to provide the title compound (0.20 g, 47% yield): ES-MS (m z) 457
[M+H]+. E. 2-Phenyl-l-H-[(2-piperidyl)ethoxy]benzyl}-1.2.3,4-tetrahydroisoquinoline-6-ol
The title compound was prepared as described in Example 2, using 6- methoxy-2-phenyl-l-{4-[(2-piperidyl)ethoxy]benzyl}-l,2,3,4-tetrahydro-isoquinoline
(0.08 g, 0.16 mmol) to afford 6-hydroxy-2-phenyl-l-{4-[(2-piperidyl)ethoxy]benzyl}-
1,2,3,4-tetrahydroisoquinoline (0.030 g, 42% yield): 1H NMR (CD3OD) 7.13 (dd, 2H), 7.03 (d, 2H), 6.94 (d,2H), 6.91 (dd, 4H), 6.64 (m, 2H), 4.78 (t, IH), 4.29 (m, 2H), 3.3- 36 (m, 6H), 3.1 1 (dd, IH), 3.00 (dd, IH), 2.80 (m, IH), 2.57 (m, IH), 1.84 (m, 6H), 1.15 (t, 2H); ES-MS (m z) 443 [M+H]+.
EXAMPLE 4
SYNTHESIS OF 2-(4-FLUOROPHENYL)-6-METHOXY-1-{4-[(2-
PIPERIDYL)ETHOXY]BENZYL} - 1 ,2,3,4-TETRAHYDROISOQUINOLINE
A. N-(4-Fluorophenyl)-2-(3-methoxyphenyl)acetamide
The title compound was prepared as described in Example LA, using 3- methoxyphenylacetyl chloride (3.29 g, 18.0 mmol) and 4-fluoroaniline (1.98 g, 18.0 mmol) to afford the title compound (4.57 g, 98% yield): ES-MS (m/z) 259.
B. (4-Fluorophenyl) {2-(3-methoxyphenyl)ethyl| amine The title compound was prepared as described in Example l.B, using N-
(4-fluorophenyl)-2-(3-methoxyphenyl)acetamide (4.57 g, 17.6 mmol). Chromatography (SiO2, 5:1 hexanes/ethyl acetate) of the crude mixture afforded the title compound (3.84 g, 52% yield): ES-MS (m z) 245.
C. N-(4-Fluorophenyl)-N-{2-(3-methoxyphenyl)ethyl}-2-{4- (phenylmethoxy)phenyl } acetamide
The title compound was prepared as described in Example 1.C, using (4- fluorophenyl){2-(3-methoxyphenyl)ethyl} amine (14.2 g, 58 mmol) and 4- benzyloxyphenylacetyl chloride (15.1 g, 58 mmol) prepared from the corresponding carboxylic acid (14.0 g, 58 mmol) and oxalyl chloride (6.5 mL, 75 mmol) in CH2C12 (150 mL) (19.1 g, 70% yield): ES-MS (m/z) 470 [M+H]+.
D. 2-(4-Fluorophenyl)-6-methoxy- 1 - |4-(phenylmethoxy) benzyl } - 1 ,2,3,4- tetrahydroisoq uinoline
A solution of N-(4-fluorophenyl)-N-{2-(3-methoxyphenyl)ethyl}-2-{4-
(phenylmethoxy)phenyl} acetamide (6.0 g, 12.8 mmol) in phosphorous oxychloride (130 mL) under nitrogen was heated to 80°C. After 20 hours, the reaction was cooled to RT and very slowly poured over ice with vigorous stirring. Ethyl acetate (500 mL)
was then added and the layers were separated. The organic layer was washed with brine, dried over MgSO4, filtered and concentrated to provide the title compound (4.61 g, 80% yield): ES-MS (m/z) 452 [M+H]+.
E. 2-(4-Fluorophenyl)- 1 -(4-hydroxybenzyl)-6-methoxy- 1 ,2,3,4- tetrahydroisoquinoline
The title compound was prepared as described in Example 3.C, using 2- (4-fluorophenyl)-6-methoxy- 1 - {4-(phenylmethoxy)phenylmethylene} - 1 ,2,3 ,4- tetrahydroisoquinoline (4.0 g, 8.87 mmol). Chromatography (SiO2, 2:1 hexanes/ethyl acetate) provided the title compound (1.0 g, 31% yield): ES-MS (m z) 364 [M+H]+. F. 2-(4-Fluorophenyl)-6-methoxy-l-{4- (2-piperidyl)ethoxylbenzyl} -1,2,3,4- t trahvdro isoq uinolin
The title compound was prepared as described in Example 3.D, using 2- (4-fluorophenyl)-l-(4-hydroxybenzyl)-6-methoxy-l,2,3,4-tetrahydroisoquinoline (1.0 g, 2.75 mmol) to provide the title compound (1.28 g, 98% yield): ES-MS (m/z) 475
EXAMPLE 5 SYNTHESIS OF 2-(4-FLUOROPHENYL)- 1 - {4-[(2-PIPERIDYL) ETHOXYJBENZYL}- 1,2,3,4-
TETRAHYDROISOQUINOLIN-6-OL
The title compound was prepared as described in Example 3.E, using 2-
(4-fluorophenyl)-6-methoxy-l-{4-[(2-piperidyl)ethoxy]benzyl}-l,2,3,4- tetrahydroisoquinoline (1.28 g, 2.7 mmol) to afford the title compound (0.42 g, 34% yield): Η NMR (CDC13) 6.5-7.0 (m, 1 IH), 4.68 (t, IH), 4.07 (m, 2H), 3.4-3.5 (m, 3H), 3.06 (m, IH), 2.5-2.9 (m, 8H), 1.46 (m, 4H), 1.26 (m, 2H); ES-MS (m/z) 461 [M+H]+.
EXAMPLE 6
SYNTHESIS OF 6-METHOXY-2- {5-(2-METHOXYPYRIDINE)}-1 - {4-[(2-
PIPERIDYL)ETΉOXY]BENZYL} - 1 ,2,3,4-TETRAHYDROISOQUINOLINE
A. 2-(3-Methoxyphenyl)-N-{2-methoxy(5-pyridyl)} acetamide
The title compound was prepared as described in Example LA, using 3- methoxyphenylacetyl chloride (4.8 g, 26.0 mmol) and 5-amino-2-methoxypyridine (3.23 g, 26.0 mmol) to afford the title compound (7.0 g, 99% yield): ES-MS (m/z) 272.
B. {2-(3-Methox phenyl)ethyl}-N-{2-methoxy(5-pyridyl)} amine The title compound was prepared as described in Example LB, using 2-
(3-methoxyphenyl)-N-{2-methoxy(5-pyridyl)} acetamide (7.0 g, 25.7 mmol). Chromatography (Siθ2, 5: 1 hexanes/ethyl acetate) afforded the title compound (3.96 g, 60% yield): ES-MS (m/z) 258.
C. N-{2-Methoxy(5-pyridyl)}-N-{2-(3-methoxyphenyl)ethyl}-2-{4- (phenylmethoxy)phenyl } acetamide
The title compound was prepared as described in Example 3. A, using {2- (3-methoxyphenyl)ethyl}-N-{2-methoxy(5-pyridyl)} amine (3.3 g, 12.8 mmol) to afford the title compound (5.0 g, 81% yield): ES-MS (m/z) 483 [M+H]+.
D. l-{4-(Phenylmethoxy)benzyl}-6-methoxy-2-{5-(2-methoxypyridyl)} -1,2,3,4- tetrahydroisoquinoline
The title compound was prepared as described in Example 1.D, using N- (2-methoxy(5-pyridyl)} -N- {2-(3-methoxyphenyl)ethyl} -2- {4-(phenylmethoxy) phenyl} acetamide (3.67 g, 7.61 mmol) to provide the title compound (2.7 g, 76% yield): ES-MS (m/z) 467 [M+H]+.
E. l-(4-Hydroxybenzyl)-6-methoxy-2-{5-(2-methoxypyridyl)}-l,2,3,4- tetrahydroisoquinoline
The title compound was prepared as described in Example 3.C, using 1-
{4-(phenylmethoxy)benzy 1 } -6-methoxy-2- { 5-(2-methoxypyridyl) } - 1 ,2,3 ,4- tetrahydroisoquinoline (0.87 g, 1.86 mmol) to afford the title compound (0.63 g, 90% yield): ES-MS (m/z) 377 [M+H]+.
F. 6-Methoxy-2- {5-(2-methoxypyridine) } - 1 - {4-f (2-piperidyl)ethoxy~lbenzyl} - 1,2,3,4-tetrahydroisoquinoline
The title compound was prepared as described in Example 3.D, using 1- (4-hydroxybenzyl)-6-methoxy-2- {5-(2-methoxypyridyl)} -1 ,2,3,4- tetrahydroisoquinoline (0.60 g, 1.6 mmol) to afford the title compound (0.61 g, 78% yield): ES-MS (m/z) 488 [M+H]+.
EXAMPLE 7 SYNTHESIS OF 2- { 5-(2-METHOX YP YRIDINE) } - 1 - {4- [(2-PIPERID YL)ETHOXY] BENZYL } - L,2,3,4-TETRAHYDROISOQUINOLIN-6-OL
The title compound was prepared as described in Example 2, using 6- methoxy-2-{5-(2-methoxypyridine)}-l-{4-[(2-piperidyl)ethoxy]beri2yl}-l, 2,3,4- tetrahydroisoquinoline (0.2 g, 0.41 mmol) to afford the title compound (0.017 g, 9% yield): ES-MS (m/z) 474 [M+H]+.
EXAMPLE 8 SYNTHESIS OF 2-FLUOROPHENYL-l {4-[(2-PIPERIDYL)ETHOXY]BENZYL}-1H, 3H, 4H, 5H-
BENZO(E)AZEPIN-7-YL
A. N-(4-Fluorophenyl)-3-(3-methoxyphenyl)propanamide
The title compound was prepared as described in Example 1.A, using 3- methoxyphenylpropionylchloride (6.62 g, 33.3 mmol) and 4-fluoroaniline (3.70 g, 33.3 mmol) to afford N-(4-fluorophenyl)-3-(3-methoxyphenyl)propanamide (8.85 g, 97%> yield): ES-MS (m/z) 273. B. (4-Fluorophenyl)[3-(3-methoxyphenyl)propyl]amine
The title compound was prepared as described in Example 1.B, using N- (4-fluorophenyl)-3-(3-methoxyphenyl)propanamide (2.0 g, 7.32 mmol) to afford (4- fluorophenyl)[3-(3-methoxyphenyl)propyl]amine (1.85 g, 97% yield): ES-MS (m/z) 259. C. N-(4-Fluorophenyl)-2-(4-methoxyphenyl)-N-r3-(3- methoxyphenyl)propyl~|acetamide
The title compound was prepared as described in Example LC, using (4- fluorophenyl)[3-(3-methoxyphenyl)propyl]amine (1.0 g, 4.13 mmol) to afford N-(4- fluorophenyl)-2-(4-methoxyphenyl)-N-[3-(3-methoxyphenyl)propyl]acetamide (1.84 g, 92% yield): ES-MS (m/z) 484 [M+H]+.
D. 2-Fluorophenyl-7-methoxy-l-{4-r(2-piperidyl)ethoxylbenzyl}-lH, 3H, 4H, 5H- benzo(e)azepine
The title compound was prepared as described in Example 4.D, using N-
(4-fluorophenyl)-2-(4-methoxyphenyl)-N-[3-(3-methoxyphenyl)propyl]acetamide (0.80 g, 1.65 mmol) to afford l-{[2-(4-fluorophenyl)-7-methoxy(3H,4H,5H-
benzo[e]azepinylidene)]methyl}-4-(phenylmethoxy)benzene (0.50 g, 65%> yield): ES- MS (m/z) 466 [M+H]+.
E. 2-Fluorophenyl- 1 -(4-hydroxybenzyl)- 1 - {4-[(2-piperidyi)ethoxy "[benzyl) - IH, 3H, 4H, 5H-benzo(e)azepine The title compound was prepared as described in Example 3.C, using 1-
{[2-(4-fluorophenyl)-7-methoxy(3H,4H,5H-benzo[e]azepinylidene)]methyl}-4- (phenylmethoxy)benzene (0.30 g, 0.64 mmol) to afford the title compound (0.168 g, 69% yield): ES-MS (m/z) 378 [M+H]+.
F. 2-Fluorophenyl-7-methoxy-l-{4-r2-piperidyl)ethoxylbenzyl}-lH,3H,4H,5H- benzo e]azepine
The title compound was prepared as described in Example 3.D, using 2- fluorophenyl-l-(4-hydroxybenzyl)-l-{4-[(2-piperidyl)ethoxy]benzyl}-lH, 3H, 4H, 5H- benzo(e)azepine (0.15 g, 0.397 mmol) to afford the title compound (0.164 g, 87% yield): ES-MS 489 (m/z) [M+H]+. G. 2-fluoroρhenyl-l {4-f(2-piperidyl)ethoxylbenzyl}-lH, 3H. 4H, 5H- benzo(e)azepin-7-yl
The title compound was prepared as described in Example 3.E, using 2- fluorophenyl-7-methoxy- 1 - {4-[2-piperidyl)ethoxy]benzyl } - 1 H,3H,4H,5H- benzo[e]azepine (0.8 g, 0.41 mmol) to afford the title compound (0.033 g, 42% yield): ES-MS (m z) 475 [M+H]+.
EXAMPLE 9
SYNTHESIS OF 2-(4-FLUOROPHENYL)-1 - {4-[(2-DIETHYLAMINO)ETHOXY]BENZΎL}-
1,2,3,4-TETRAHYDROISOQUINΌLΓN-6-OL
A. 2-(4-Fluorophenyl)-6-methoxy- 1 - {4- (2-diethylamino)ethoxy]benzyl| - 1 ,2,3,4- tetrahydroisoquinoline
The title compound was prepared as described in Example 3.D. using 2- (4-fluorophenyl)- 1 -(4-hydroxybenzyl)-6-methoxy- 1 ,2,3 ,4-tetrahydroisoquinoline (0.13 g, 0.36 mmol) and 2-(diethylamino)ethylchloride hydrochloride (0.074 g, 0.429 mmol) to provide the title compound (0.101 g, 61% yield): ES-MS (m/z) 463 [M+H]+.
B. 2-(4-Fluorophenyl)-l-{4-r(2-diethylamino)ethoxylbenzyl}-l,2,3,4- tetrahydroisoquinolin-6-ol
The title compound was prepared as described in Example 2 using 2-(4- fluorophenyl)-6-methoxy-l-{4-[(2-diethylamino)ethoxy]benzyl}-l,2,3,4- tetrahydroisoquinoline (0.101 g, 0.218 mmol) to provide the title compound (0.021 g, 20% yield): ES-MS (m/z) 489 [M+Hf .
EXAMPLE 10 SYNTHESIS OF 2-(4-FLUOROPHENYL)- 1 - {4-[(2-DΠSOPROPYLAMΓNO)EIΉOXY]BENZYL} -
1 ,2,3,4-TETRAHYDROISOQUTNOLIN-6-OL
A. 2-(4-Fluorophenyl)-6-methoxy-l-{4-[(2-diisopropylamino)ethoxy]benzyl}- 1 ,2,3,4-tetrahydroisoquinoline
The title compound was prepared as described in Example 3.D. using 2-
(4-fluorophenyl)- 1 -(4-hydroxybenzyl)-6-methoxy- 1 ,2,3 ,4-tetrahydroisoquino line (0.13 g, 0.36 mmol) and 2-(diisopropylamino)ethylchloride hydrochloride (0.086 g, 0.429 mmol) to provide the title compound (0.091 g, 52% yield): ES-MS (m/z) 491 [M+H]+.
B. 2-(4-Fluorophenyl)-l-{4- (2-diisopropylamino)ethoxy]benzyl}-l, 2,3,4- tetrahydroisoquinolin-6-ol
The title compound was prepared as described in Example 2 using 2-(4- fluorophenyl)-6-methoxy-l-{4-[(2-diisopropylamino)ethoxy]benzyl}-l, 2,3,4- tetrahydroisoquinoline (0.091 g, 0.185 mmol) to provide the title compound (0.032 g,
36% yield): ES-MS (m/z) 477 [M+H]+.
EXAMPLE 11
SYNTHESIS OF 2-(4-FLUOROPHENYL)-1- {4-[(2-(1-METHYLPYRROLIDIN-2-
YL))ETHOXY]BENZYL}-1 ,2,3,4-TETRAHYDROISOQUΓNOLIN-6-OL
A. 2-(4-Fluorophenyl)-6-methoxy- 1 - {4-[(2-( 1 -methylpyrrolidin-2- yl))ethoxylbenzyl}-l,2,3,4-tetrahydroisoquinoiine
The title compound was prepared as described in Example 3.D. using 2-
(4-fluorophenyl)- 1 -(4-hydroxybenzyl)-6-methoxy- 1 ,2,3 ,4-tetrahydroisoquinoline (0.13 g, 0.36 mmol) and 2-(2-chloroethyl)-l-methylpyrrolidine hydrochloride (0.079 g, 0.429 mmol) to provide the title compound (0.076 g, 45% yield): ES-MS (m/z) 475 [M+H]+.
B. 2-(4-Fluorophenyl)- l-(4-|"(2-(l-methylpyrrolidin-2-yl))ethoxylbenzyl|-l,2,3,4- tetrahydroisoquinolin-6-ol
The title compound was prepared as described in Example 2 using 2-(4- fluorophenyl)-6-methoxy-l-{4-[(2-(l-methylpyrrolidin-2-yl))ethoxy]benzyl} -1,2,3,4- tetrahydroisoquinoline (0.076 g, 0.160 mmol) to provide the title compound (0.01 1 g,
15% yield: ES-MS (m/z) 461 [M+H]+.
EXAMPLE 12 SYNTHESIS OF 2-(4-FLLΌROPHENYL)- 1 - {4-[(2-PYRROLIDINYL)ETHOXY]BENZYL} - 1 ,2,3,4-
TETRAHYDROISOQUINOLIN-6-OL
A. 2-(4-Fluorophenyl)-6-methoxy- 1 - {4-[(2-pyrrolidinyl)ethoxy]benzyl } - 1 ,2,3 ,4- tetrahvdroiso uinoline
The title compound was prepared as described in Example 3.D. using 2-
(4-fluorophenyl)- 1 -(4-hydroxybenzyl)-6-methoxy- 1 ,2,3,4-tetrahydroisoquinoline (0.13 g, 0.36 mmol) and l-(2-chloroethyl)pyrrolidine hydrochloride (0.073 g, 0.429 mmol) to provide the title compound (0.109 g, 66% yield): ES-MS (m/z) 461 [M+H]+.
B. 2-(4-Fluorophenyl)-l-{4-|"(2-pyrrolidinyl)ethoxy1benzyl}-l,2,3,4- tetrahydroisoquinolin-6-ol
The title compound was prepared as described in Example 2 using 2-(4- fluorophenyl)-6-methoxy-l-{4-[(2-pyrrolidinyl)ethoxy]benzyl}-l,2,3,4- tetrahydroisoquinoline (0.109 g, 0.237 mmol) to provide the title compound (0.036 g, 34% yield): ES-MS (m/z) 447 [M+H]+.
EXAMPLE 13 SYNTHESIS OF 1- {4-[(2-AZAPERHYDROEPINYL)ETHOXY]BENZYL}-2-(4-FLUOROPHENYL)-
L ,2,3,4-TETRAHYDR0ISOQUINOLIN-6-OL
A. 1 - {4-|"(2-Azaperhydroepinyl)ethoxy'|benzyl } -2-(4-fluorophenyl)-6-methoxy- 1.2,3,4-tetrahydroisoquinoline
The title compound was prepared as described in Example 3.D. using 2-
(4-fluorophenyl)-l -(4-hydroxybenzyl} -6-methoxy-l ,2,3,4-tetrahydroisoquinoline (0.13 g, 0.36 mmol) and 2-(hexamethylimino)ethylchloride hydrochloride (0.085 g, 0.429 mmol) to provide the title compound (0.105 g, 60% yield): ES-MS (m/z) 489 [M-rH]+.
B. l-{4- (2-Azaperhydroepinyl)ethoxylbenzyl}-2-(4-fluorophenyl)- 1,2,3,4- tetrahydroisoquinolin-6-ol
The title compound was prepared as described in Example 2 using l-{4-
[(2-azaperhydroepinyl)ethoxy]benzyl}-2-(4-fluorophenyl)-6-methoxy-l, 2,3,4- tetrahydroisoquinoline (0.105 g, 0.215 mmol) to provide the title compound (0.020 g,
20% yield: ES-MS (m/z) 475 [M+H]+.
EXAMPLE 14
SYNTHESIS OF 2-(METHYLETHYL 1 - {4-[(2-PIPERIDYL)ETHOXY]BENZYL} - 1 ,2,3,4-
TETRAHYDROISOQUINOLIN-6-OL TRIFLUOROACETATE
Scheme for Examples 14, 15, 16, 19 and 20
A. N-[2-(3-Methoxyphenyl)ethyl]-2-[4-(phenylmethoxy)phenyllacetamide
To a solution of 4-benzyloxyphenylacetic acid (4.85 g 20 mmol) in dimethylformamide (30 mL) under nitrogen was added 1 ,3-diisopropylcarbodiimide. After 2 hours, to the solution was added 2-(3-methoxyphenyl)ethylamine (3.02 g, 20 mmol) and stirred at room temperature for 20 hours. The reaction was quenched with a saturated sodium carbonate solution and extracted with ethyl acetate. The organic layer was dried over MgSO , filtered, and concentrated. The residue was then purified by chromatography (SiU2, 30-70% ethyl acetate/hexane) to provide the title compound (5.74 g, 76% yield): Η NMR (CDC13) 7.38 (m, 5H), 7.14 (t, IH), 7.07 (d, 2H), 6.91 (d, 2H), 6.74 (dd, IH), 6.62 (m, 2H), 5.37 (br, IH), 5.06 (s, 2H), 3.77 (s, 3H), 3.47 (s, 2H), 3.44 (t, 2H), 2.70 (t, 2H); ES-MS (m/z) 376 [M+H]+.
B. 6-Methoxy-l-[4-(phenylmethoxy)berιzyl]-l,2,3,4-tetrahydroisoquinoline
A solution of N-[2-(3-methoxyphenyl)ethyl]-2-[4-
(phenylmethoxy)phenyl]acetamide (5.739 g, 15.3 mmol) and phosphorous oxychloride (15 mL) in acetonitrile (40 mL) under nitrogen was heated at 80 °C for 5 hours. Solvents were evaporated. Ethyl acetate was added and evaporated three times. The residue was dissolved in methanol (50 mL) and sodium borohydride (2.00 g, 52.9 mmol) was carefully added to the solution in small portions. After 2 hours, the reaction was quenched with water and extracted with CH2CI2. The organic layer was dried over MgSO , filtered, and concentrated. The residue was then purified by chromatography (Siθ2, 0-10% methanol/CTLCb) to provide the title compound (1.54 g, 28% yield): 1H NMR (CDC13) 7.36 (m. 6H), 7.12 (d, 2H), 6.91 (d. 2H), 6.73 (dd, IH), 6.62 (m, IH), 5.04 (s, 2H), 4.97 (t, IH), 4.17 (br, IH), 3.78 (s, 3H), 3.73 (m, IH), 3.16 (m, 2H), 2.83 (m, 3H); ES-MS (m/z) 360 [M+H]+.
C. 6-Methoxy-2-(methylethyl)-l-[4-(phenylmethoxy)benzyl~]-l, 2,3,4- tetrahydroisoquinoline
To a mixture of 6-methoxy-l-[4-(phenylmethoxy)benzyl]-l,2,3,4- tetrahydroisoquinoline (0.36 g, 1 mmol), acetone (3 mL), and sodium dihydrogenphosphate (0.4 g) in methanol (5 mL) was added sodium cyanoborohydride (0.5 g, 8 mmol). After 48 hours, the reaction was quenched with water and extracted with CH2CI2. The organic layer was dried over MgSO4, filtered, and concentrated to give the title compound (0.321 g, 80% yield): ES-MS (m/z) 402 [M+H]+.
D. 6-Methoxy-2-(methylethyl)-l-(4-hydroxybenzyl)-l,2,3,4-tetrahydroisoquinoline
A suspension of 6-methoxy-2-(methylethyl)-l-[4-
(phenylmethoxy)benzyl]-l,2,3,4-tetrahydroisoquinoline (0.3 g, 0.75 mmol), palladium (10% wt) on activated carbon (0.06 g) and acetic acid (5 drops) in ethyl acetate (10 mL) was stirred under hydrogen overnight. The reaction was filtered and concentrated to provide the title compound (0.212 g, 91% yield): ES-MS (m/z) 312 [M+H]+.
E. 6-Methoxy-2-(methylethyl)-l - {4-["(2-piperidyl)ethoxy]bεnzyl} - 1 ,2,3.4- tetrahydroisoquinoline A mixture of 6-methoxy-2-(methylethyl)-l-(4-hydroxybenzyl)- 1,2,3,4- tetrahydroisoquinoline (0.212 g, 0.68 mmol), 2-chloroethylpiperidine hydrochloride
(0.25 g, 1.36 mmol), and potassium carbonate (0.47 g, 3.4 mmol) in dimethylformamide (10 mL) was heated at 80 °C overnight. After cooling to room temperature, the mixture was poured into water and extracted with CH2CI2. The organic layer was dried over MgSO4, filtered, and concentrated. The residue was then purified by chromatography (SiO2, 0-15% methanol/CH2Cl2) to provide the title compound (0.201 g, 70% yield): ES-MS (m/z) 423 [M+H]+.
F. 2-(Methylethyl)- 1 - {4-r(2-piperidyl)ethoxylbenzyl} - 1 ,2,3 ,4- tetrahydroisoquinolin-6-ol Trifluoro acetate
To a solution of 6-methoxy-2-(methylethyl)-l-{4-[(2- piperidyl)ethoxy]benzyl}-l,2,3,4-tetrahydroisoquinoline (0.2 g, 0.47 mmol) in CH2CI2 (8 mL) at -15 °C under nitrogen was added a solution of 1.0 M boron tribromide (1.4 mL, 1.4 mmol). After stirring at -15°C for 2 hours and at 0 °C for 2 hours, the reaction w::? poured into an ice and saπ.rateri me i bicarbonate solution and extracted with ethyl acetate. The organic ) er was dried
er MgSO-,. filtered, and concentrated. The residue was then purified by HPLC (C-18 column, 10-100% acetonitrile/water with 0.1%) trifluoroacetic acid) to provide the title compound (0.084 g, 43% yield): 1H NMR (DMSO-d6) 9.65 (br, 2H), 6.93-7.06 (m, 4H), 6.66 (s, IH), 6.33 (m, 2H), 4.62 (t, IH), 4.34 (m, 3H), 3.96-3.00 (m 12H), 1.76 (m, 4H), 1.47 (m, 2H), 1.30 (d, 6H); ES-MS (m/z) 409 [M+H]+.
EXAMPLE 15
SYNTHESIS OF 2-CYCLOPENTΎL- 1 - {4-[(2-PIPERIDYL)ETHOXY]BENZYL} -1 ,2,3,4-
TETRAHYDROISOQUINOLIN-6-OL TRIFLUOROACETATE
A. 2-Cyclopentyl-l-methoxy-l-[4-(phenylmethoxy)benzyl~]-l,2,3,4- tetrahvdroisoquinoline
The title compound was prepared as described in Example 14.C, using 6- methoxy-l-[4-(phenylmethoxy)ber:zyl]-l ,2.?.4-tetrahydroisoqumoline (0.5 g, 1.39 mmol) and cyclopentanone (0.951 g, 11.3 mmol) to provide the title compound (0.495 g, 83% yield): ES-MS (m/z) 42S [M+H]~.
B. 2-Cyclopentyl-6-l-(4-hydroxybenzyl)-6-methoxy-l,2,3,4-tetrahydroisoquinoline
The title compound was prepared as described in Example 14.D, using 2- cyclopentyl-6-methoxy-l-[4-(phenylmethoxy)benzyl]-l,2,3,4-tetrahydroisoquinoline (0.495 g, 1.15 mmol) to provide the title compound (0.31 1 g, 79%> yield): ES-MS (m/z) 338 [M+H]+.
C. 2-Cyclopentyl-6-methoxy-l-{4-[(2-piperidyl)ethoxy]benzyl}-l,2,3,4- tetrahydroisoquinoline
The title compound was prepared as described in Example 14.E, using 2-
(cyclopentyl)- 1 -(4-hydroxybenzyl)-6-methoxy- 1 ,2,3 ,4-tetrahydroisoquinoline (0.31 g, 0.92 mmol) to provide the title compound (0.313 g, 76% yield): ES-MS (m/z) 449
[M+H]+.
D. 2-Cyclopentyl-l-{4-[(2-piperidyl)ethoxy1benzyl}-l,2,3,4-tetrahydroisoquinolin- 6-ol Trifluoroacetate
The title compound was prepared as described in Example 14.F, using 2- cyclopentyl-6-methoxy-l- {4-[(2-piperidyl)ethoxy]benzyl}- 1,2,3,4- tetrahydroisoquinoline (0.31 g, 0.7 mmol) to provide the title compound (0.16 g, 53%
yield): 1H NMR (DMSO-d6) 9.87 (br, IH), 9.56 (br, IH), 6.87-7.06 (m, 4H), 6.62 (s, IH), 6.36 (dd, IH), 6.15 (dd, IH), 4.48 (t, IH), 4.29 (t, 2H), 3.94 (m, IH), 2.8-3.8 (m 12H), 1.98-2.22 (m, 2H), 1.4-1.8 (m, 12H); ES-MS (m/z) 435 [M+H]+.
EXAMPLE 16
SYNTHESIS OF 1 - {4-[(2-PIPERIDYL)ETHOXY]BENZYL} -2-(TETRAHYDROPYRAN-4-YL)-
1 ,2,3,4-TETRAHYDROISOQUINOLIN-6-OL TRIFLUOROACETATE
A. 6-Methoxy-l-[4-(phenylmethoxy)benzyl]-2-(tetrahydropyran-4-yl)-l,2,3,4- tetrahydroisoquinoline The title compound was prepared as described in Example 14.C, using 6- methoxy-l-[4-(phenylmethoxy)benzyl]-l,2,3,4-tetrahydroisoquinoline (0.5 g, 1.39 mmol) and tetrahydro-4H-pyran-4-one (1.084 g, 10.8 mmol) to provide the title compound (0.479 g, 78% yield): ES-MS (m/z) 444 [M+H]+.
B. l-(4-Hydroxybenzyl)-6-methoxy-2-(tetrahydropyran-4-yl)-l,2,3,4- tetrahydroisoquinoline
The title compound was prepared as described in Example 14.D, using 6- methoxy-l-[4-(phenylmethoxy)benzyl]-2-(tetrahydropyran-4-yl)-l, 2,3,4- tetrahydroisoquinoline (0.47 g, 0.1 mmol) to provide the title compound (0.324 g, 85% yield): ES-MS (m/z) 354 [M+H]+. C. 6-Methoxy-l- {4-[(2-piperidyl)ethoxylbenzyl}-2-(tetrahydropyran-4-yl)-l, 2.3.4- tetrahydroisoquinoline
The title compound was prepared as described in Example 14.E, using 1-
(4-hydroxybenzyl)-6-methoxy-2-(tetrahydropyran-4-yl)-l,2,3,4-tetrahydroisoquinoline
(0.32 g, 0.92 mmol) to provide the title compound (0.342 g, 80% yield): ES-MS (m/z) 465 [M+H]+.
D. l-{4-f(2-Piperidyl)ethoxylbenzyl}-2-(tetrahydropyran-4-yl)- 1,2,3,4- tetrahydroisoquinolin-6-ol Trifluoroacetate
The title compound was prepared as described in Example 14.F, using 6- methoxy- 1 - {4-[(2-piperidyl)ethoxy]benzyl } -2-(tetrahydropyran-4-yl)- 1 ,2,3,4- tetrahydroisoquinoline (0.34 g, 0.73 mmol) to provide the title compound (0.156 g, 47% yield): Η NMR (DMSO-d6) 9.79 (br, IH), 9.6 (br, IH), 6.91-7.07 (m, 4H), 6.66 (s, IH),
6.05-6.43 (m, 2H), 4.69 (t, IH), 4.31 (t, 2H), 2.99-4.0 (m 12H), 2.2 (m, IH), 2.06 (m,
4H), 1.5-1.86 (m, 8H),1.41 (m, 2H); ES-MS (m z) 451 [M+Hf.
EXAMPLE 17 SYNTHESIS OF 2-(4-FLUOROPHENYL)- 1 - {4-[(2-MORPHOLINYL)ETHOXY]BENZYL} -1 ,2,3,4-
TETRAHYDROISOQUINOLIN-6-OL
A. 2-(4-FIuorophenyl)-6-methoxy-l-{4- (2-morpholinyl)ethoxylbenzyl} -1,2,3,4- tetrahydroisoquinoline The title compound was prepared as described in Example 3.D using 2-
(4-fluorophenyl)-6-methoxy- 1 - {4-hydroxybenzyl } - 1 ,2,3,4-tetrahydroisoquinoline
(0.220 g, 0.6 mmol) and 4-(2-chloroethyl)morpholine hydrochloride (0.124 g, 0.67 mmol) to provide the title compound (0.23 g, 80%> yield): ES-MS (m/z) 477 [M+H]+.
B. 2-(4-Fluorophenyl)- 1 - {4-[(2-morpholinyl)ethoxy"|benzyl } - 1 ,2,3 ,4- tetrahydroisoquinolin-6-ol
The title compound was prepared as described in Example 2, using 2-(4- fluorophenyl)-6-methoxy-l-{4-[(2-mo holinyl)ethoxy]benzyl}-l,2,3,4-tetrahydro- isoquinoline (0.23 g, 0.48 mmol) to provide the title compound (0.130 g, 46% yield):
Η NMR (CDC13) 6.9(m, 4H), 6.75(m, 3H), 6.6(m,4H),4.7(t, IH), 4.1(m, 2H), 3.74(m, 4H), 3.5(m, 2H), 3.1(m, IH), 2.9(m, 2H), 2.8(m, 2H), 2.6(m, IH), 2.6(m, 4H); ES-MS
(m z) 463 [M+H]+.
EXAMPLE 18 SYNTHESIS OF 2-(4-FLUOROPHENYL)- 1 - {3-[(2-PIPERIDYL)ETHOXY] BENZYL }- 1,2,3 ,4-
TETRAHYDROISOQUINOLIN-6-OL
A. N-{2-(3-Methoxyphenyl)ethyl}-N-(4-fluorophenyl)-2-{3-hydroxyphenyl}- acetamide
The title compound was prepared as described in Example 34. B using 3- hydroxyphenylacetic acid (0.456 g, 3 mmol) and 4-fluorophenyl)-{2-(3- methoxyphenyl)ethyl} amine (0.73 g, 3 mmol) to provide the title compound (0.7 g, 62% yield): ES-MS (m/z) 380 [M+Hf.
B. 2-(4-Fluorophenyl)- 1 -(3-hydroxybenzyl)-6-methoxy- 1 ,2,3 ,4- tetrahydroisoquinoline
The title compound was prepared as described in Example 1.D, using N- {2-(3-methoxyphenyl)ethyl}-N-(4-fluorophenyl)-2-{3-hydroxyphenyl} acetamide (0.7 g, 1.8 mmol) to provide the title compound (0.15 g, 23% yield): ES-MS (m/z) 363 [M+H]+.
C. 2-(4-Fluoropheny)-6-methoxy-l-{3-[(2-piperidyl)ethoxy]benzyl}-l, 2,3,4- tetrahydroisoquinoline
The title compound was prepared as described in Example 3.D, using 2- (4-fluorophenyl)-l-(3-hydroxybenzyl)-6-methoxy-l,2,3,4-tetrahydroisoquinoline (0.15 g, 0.4 mmol) to provide the title compound (0.17 g, 89% yield): ES-MS (m/z) 475
[M+H]+.
D. 2-(4-Fluorophenyl)-l-{3-[(2-piperidyI)ethoxyl benzyl} -1 ,2,3, 4-tetrahydro- isoquinolin-6-ol The title compound was prepared as described in Example 2 using 2-(4- fluorophenyl)-6-methoxy-l -{3-[(2-piperidyl)ethoxy]benzyl}-l,2,3,4- tetrahydroisoquinoline (0.174 g, 0.37 mmol). Purification by column chromatography
(SiO2, ethyl acetate:ethanol, 8:2) provided the title compound (0.027 g, 16% yield): ES- MS (m/z) 461 [M+H]".
EXAMPLE 19
SYNTHESIS OF 2-METHYL- 1 - {4-[(2-PIPERIDYL)ETHOXY]BENZYL}- 1,2,3,4-
TETRAHYDROISOQUINOLIN-6-OL TRIFLUOROACETATE
A. 6-Methoxy-2-methyl- 1 -|"4-(phenylmethoxy)benzyl]- 1 ,2,3,4- tetrahydroisoquinoline
The title compound was prepared as described in Example 14. B, providing the title compound (0.854 g, 0.015% yield).
B. l-(4-Hydroxybenzyl)-6-methoxy-2-methyl-l,2,3,4-tetrahydroisoquinoline
The title compound was prepared as described in Example 14.D, using 6- methoxy-2-methyl-l-[4-(phenylmethoxy)benzyl]-l,2,3,4-tetrahydroisoquinoline (0.84 g, 2.25 mmol) to providε the title compound (0.534 g, 84% yield): ES-MS (m/z) 284 [M+H]+.
C. 6-Methoxy-2-methyl-l-{4-[(2-piperidyl)ethoxy]benzyl}-l, 2,3,4- tetrahydroisoquinoline
The title compound was prepared as described in Example 14.E, l-(4- hydroxybenzyl)-6-methoxy-2-methyl-l,2,3,4-tetrahydroisoquinoline (0.534 g, 1.88 mmol) to provide the title compound (0.216 g, 29% yield): ES-MS (m/z) 395 [M+H]".
D. 2-Methyl- l-{4-[(2-piperidyl)ethoxy]benzyl}-l, 2, 3.4-tetrahydroisoquinolin-6-ol Trifluoroacetate
The title compound was prepared as described in Example 14. F, using 6- methoxy-2-methyl-l -{4-[(2-piperidyl)ethoxy]benzyl}-l,2,3,4-tetrahydroisoquinoline
(0.20 g, 0.507 mmol) to provide the title compound (0.103 g, 54% yield): ES-MS (m/z) 381 [M+H]+.
EXAMPLE 20
SYNTHESIS OF 2-CYCLOHEXYL- I - {4-[(2-PIPERIDYL)ETHOXY]BENZYL}- 1,2,3,4-
TETRAHYDROISOQUINOLIN-6-OL TRIFLUOROACETATE
A. 2-Cyclohexyl-6-methoxy-l-[4-(phenylmethoxy)benzyl]- 1,2,3,4- tetrahydroisoquinoline
The title compound was prepared as described in Example 14.C, using 6- methoxy-l-[4-(phenylmethoxy)benzyl]-l,2,3,4-tetrahydroisoquinoline (0.5 g, 1.39 mmol) and cyclohexanone (0.588 g. 6.0 mmol) to provide the title compound (0.324 g,
53% yield): ES-MS (m/z) 442 [M+H]+.
B. 2-Cyclohexyl-l-(4-hydroxybenzyl)-6-methoxy-l,2,3,4-tetrahydroisoquinoline
The title compound was prepared as described in Example 14.D, using 2- cyclohexyl-6-methoxy-l-[4-(phenylmεthoxy)benzyl]-l,2,3,4-tetrahydroisoquinoline (0.32 g, 0.73 mmol) to provide the title compound (0.124 g, 48% yield): Η NMR (CDC13) 6.86 (d, 2H), 6.70 (d, 2H), 6.58 (m, 4H), 4.06 (t, IH), 3.76 (s, 3H), 3.24 (m, IH), 3.04 (m, 2H), 2.75 (m, 2H), 2.54 (m, 2H),1.69-1.87 (m, 4H), 1.58 (m, IH), 1.13-1.25 (m, 5H); ES-MS (m/z) 352 [M+H]+. C. 2-Cyclohexyl-6-methoxy-l- {4-[(2-piperidyl)ethoxy]benzyl}-l,2,3,4- tetrahydroisoquinoline
The title compound was prepared as described in Example 14.E, using 2- cyclohexyl- 1 -(4-hydroxybenzyl)-6-hydroxy- 1 ,2,3,4-tetrahydroisoquinoline (0.124 g,
0.35 mmol) to provide the title compound (0.95 g, 59% yield): ES-MS (m/z) 463 [M+H]+.
D. 2-Cyclohexyl-l-{4- (2-piperidyl)ethoxy]benzyl}-l,2,3,4-tetrahydroisoquinolin- 6-ol Trifluoroacetate
The title compound was prepared as described in Example 14.F, using 2- cyclohexyl-6-methoxy- 1 - {4-[(2-piperidyl)ethoxy]benzyl} - 1 ,2,3,4- tetrahydroisoquinoline (0.95 g, 0.2 mmol) to provide the title compound (0.052 g, 57% yield): 1H NMR (CDC13) 11.65 (br, IH), 11.2 (br, IH), 6.79 (d, 2H), 6.73 (d, IH), 6.67
(d, 2H), 6.54 (dd, IH), 6.07 (d, IH), 4.45 (dd, IH), 4.28 (t, 2H), 3.70 (m, 3H), 3.55 (dd,
IH), 3.44 (t, 2H), 2.71-3.08 (m 6H), 1.87-2.16 (m, 9H), 1.6 (m, 4H), 1.4 (m, 1H),1.2
(m, 3H); ES-MS (m/z) 449 [M+H]+.
EXAMPLE 21
SYNTHESIS OF 1 - {4-[(2-(N-BENZYL-N-ETHYL)AMINO)ETHOXY]BENZYL} -2-(4- FLUOROPHENYL)-! ,2,3 ,4-TETRAHYDROISOQUINOLIN-6-OL
A. 1 - {4-[(2-(N-benzyl-N-ethyl)amino)ethoxy]benzyl } -2-(4-fluorophenyl)-6- methoxy-l,2,3,4-tetrahydroisoquinoline
The title compound was prepared as described in Example 3.D using N- (2-chloroethyl)-N-ethyl-benzylamine hydrochloride (0.1 15 g, 0.5 mmol) to provide the title compound (0.18 g, 77% yield): ES-MS (m/z) 525 [M+H]+.
B. 1 - {4-[(2-(N-benzyl-N-ethyl)amino)ethoxy]benzyl } -2-(4-fluorophenyl)- 1 ,2,3,4- tetrahydroisoquinolin-6-ol
The title compound was prepared as described in Example 2 using l-{4- [(2-(Tsl-benzyl-N-ethyl)amino)ethoxy]benzyl}-6-methoxy-2-(4-fluoropheny)-l,2,3,4- tetrahydroisoquinoline (0.11 g, 0.2 mmol). Purification by preparative HPLC (C-18 column, 10-100% acetonitrile/water with 0.1% trifluoroacetic acid) provided the title compound (0.045 g, 20 % yield): m.p. 47-49°C; ES-MS (m/z) 511 [M+H]+.
EXAMPLE 22
SYNTHESIS OF 2-(4-FLUOROBENZOYL)-1 - {4-[(2-PIPEPJD YL)ETHOXY]BENZYL} -1 , 2,3,4-
TETRAHYDROISOQLTNOLIN-6-OL TRIFLUOROACETATE
Reaction Scheme
Scheme for Examples 22, 23, 24, 25 and 27
Examples 22, 23 & 24
Examples 25 & 27
A. 2-(4-Fluorobenzoyl)-6-methoxy-l-[4-(phenylmethoxy)benzyl]-l,2,3,4- tetrahydroisoquinoline
The title compound was prepared as described in Example 24. A, using 6- methoxy-l-[4-(phenylmethoxy)benzyl]-l, 2,3, 4-tetrahydroisoquino line (0.72 g, 2.0 mmol) and 4-fluorobenzoyl chloride (0.475 g, 3.0 mmol) to provide the title compound
(0.786 g, 82% yield): ES-MS (m/z) 482 [M+H]+.
B. 2-(4-Fluorobenzoyl)-l-(4-hydroxybenzyl)-6-methoxy-l, 2.3,4- tetrahydroisoquinoline
The title compound was prepared as described in Example 14.D, using 2- (4-fluorobenzoyl)-6-methoxy-l-[4-(phenylmethoxy)benzyl]-l, 2,3,4- tetrahydroisoquinoline (0.74 g, 1.54 mmol) to provide the title compound (0.563 g, 94% yield): Η NMR (CDC ) 7.26-7.37 (m, 2H), 7.41 (br, IH), 7.01-7.15 (m, 3H), 6.61-6.92 (m, 7H), 6.00 (dd, IH), 4.87 (m, IH), 3.82 (s, 3H), 3.71 (m, IH), 3.47 (m, IH), 2.62-3.24 (m, 4H); ES-MS (m/z) 392 [M+H]+. C. 2-(4-Fluorobenzoyl)-6-methoxy-l-{4-[(2-piperidyl)ethoxy]benzyl] -1,2,3,4- tetrahydroisoquinoline
The title compound was prepared as described in Example 14.E, using 2- (4-fluorobenzoyl)-l-(4-hydroxybenzyl)-6-methoxy-l,2,3,4-tetrahydroisoquinoline (0.51 g, 1.3 mmol) to provide the title compound (0.601 g, 92% yield): ES-MS (m/z) 503 [M+H]+.
D. 2-(4-Fluorobenzoyl)-l-{4-[(2-piperidyl)ethoxy]benzyl}-l,2,3,4- tetrahydroisoquinolin-6-ol Trifluoroacetate
The title compound was prepared as described in Example 14.F, using 2- (4-fluorobenzoyl)-6-methoxy- 1 - {4-[(2-piperidyl)ethoxy]benzyl } - 1 ,2,3,4- tetrahydroisoquinoline (0.60 g, 1.19 mmol) to provide the title compound (0.279 g, 48% yield): Η NMR (DMSO-d6) 9.55 (br, 2H), 7.21 (m, 2H), 6.92-7.10 (m, 5H), 6.52-6.64 (m, 3H), 5.69 (t, IH), 4.6 (dd, IH), 4.29 (t, 2H), 3.3-3.65 (m, 5H), 2.56-3.16 (m, 7H), 1.41-1.80 (m, 6H); ES-MS (m/z) 489 [M+H]+.
EXAMPLE 23
SYNTHESIS OF 2-(4-H YDROXYBENZOYL)-1 - {4-[(2-PIPERIDYL)ETHOXY]BENZYL}- 1,2,3,4-
TETRAHYDROISOQUINOLIN-6-OL TRIFLUOROACETATE
A. 6-Methoxy-2-(4-methoxybenzoyl)-l-[4-(phenylmethoxy)benzyl]- 1,2,3,4- tetrahvdroisoquinoline
The title compound was prepared as described in Example 24.A, using 6- methoxy-l-[4-(phenylmethoxy)benzyl]-l,2,3,4-tetrahydroisoquinoline (0.72 g, 2.0 mmol) and 4-methoxybenzoyl chloride (0.512 g, 3.0 mmol) to provide the title compound (0.717 g, 73% yield): ES-MS (m/z) 494 [M+H]+.
B. 1 -(4-Hydroxybenzyl)-6-methoxy-2-(4-methoxy 1 benzoyl)- 1 ,2,3 ,4- tetrahydroisoquinoline
The title compound was prepared as described in Example 14.D, using 6- methoxy-2-(4-methoxy 1 benzoyl)- 1 -[4-(phenylmethoxy)benzyl]- 1 ,2,3,4- tetrahydroisoquinoline (0.717 g, 1.45 mmol) to provide the title compound (0.533 g, 91% yield): 1H NMR (CDC13) 7.8 (br, IH), 7.15-7.08 (m, 3H), 6.57-6.92 (m, 7H), 6.02 (dd, IH), 4.90 (m, IH), 3.81 (s, 3H), 3.79 (s, 3H), 3.73 (m, IH), 3.47 (m, IH), 2.61-3.20 (m, 4H); ES-MS (m/z) 404 [M+H]+.
C. 6-Methoxy-2-(4-methoxybenzoyl)- 1 - {4-[(2-piperidyl)ethoxy]benzyl } - 1 ,2,3,4- tetrahydroi soq uinoline
The title compound was prepared as described in Example 14.E, using 1- (4-hydroxybenzyl)-6-methoxy-2-(4-methoxybenzoyl)- 1 ,2,3 ,4-tetrahydroisoquinoline (0.48 g, 1.19 mmol) to provide the title compound (0.541 g, 88% yield): ES-MS (m/z) 515 [M+H]+.
D. 2-(4-Hydroxybenzoyl)- 1 - {4-[(2-piperidyl)ethoxy]benzyl } - 1 ,2,3 ,4- tetrahydroisoquinolin-6-ol Trifluoroacetate
The title compound was prepared as described in Example 14.F, using 6- methoxy-2-(4-methoxybenzoyl)- 1 - {4-[(2-piperidyl)ethoxy]benzyl} - 1 ,2,3,4- tetrahydroisoquinoline (0.541 g, 1.05 mmol) to provide the title compound (0.174 g, 34% yield): 1H NMR (DMSO-d6) 9.41 (br, 2H), 7.19 (d, IH), 6.50-7.02 (m, 10H), 5.65 (t, IH), 4.5 (m, IH), 4.29 (t, 2H), 3.3-3.9 (m, 7H), 2.6-3.2 (m, 5H), 1.4-1.8 (m, 6H); ES-MS (m/z) 487 [M+H]+.
EXAMPLE 24 SYNTHESIS OF 2-BENZOYL-I - {4-[(2-PIPERIDYL)ETHOXY]BENZYL} -1,2,3,4-
TETRAHYDROISOQUINOLIN-6-OL TRIFLUOROACETATE
A. 2-Benzoyl-6-methoxy- 1 -[4-(phenylmethoxy)benzyl]- 1 ,2,3,4- tetrahydroisoquinoline To a solution of 6-methoxy-l-[4-(phenylmethoxy)benzyl]-l,2,3,4- tetrahydroisoquinoline (0.72 g, 2.0 mmol), 4-dimethylaminopyridine (0.2 g), and triethylamine (1.5 mL) in CH2CI2 (8 mL) at room temperature under nitrogen was added neat benzoyl chloride (0.42 g, 3.0 mmol) dropwise. The reaction was stirred overnight, quenched with a solution of saturated sodium bicarbonate, and extracted with CH2CI2. The organic layer was dried over MgSO , filtered, and concentrated. The residue was purified by chromatography (Siθ2, 30-50% ethyl acetate/Tiexane) to provide the title compound (0.835 g, 90% yield): ES-MS (m/z) 464 [M+H]+.
B. 2-Benzoyl-l-(4-hydroxybenzyl)-6-methoxy-l,2,3.4-tetrahydroisoquinoline
The title compound was prepared as described in Example 14.D, using 2- benzoyl-6-methoxy-l-[4-(phenylmethoxy)benzyl]-l,2,3,4-tetrahydroisoquinoline (0.8 g,
1.72 mmol) to provide the title compound (0.624 g, 97% yield): lH NMR (CDCI3) 7.26-
7.37 (m, 2H), 7.01-7.17 (m, 4H), 6.59-6.87 (m, 6H), 6.01 (t, IH), 4.88 (m, IH), 3.81 (s, 3H), 3.67 (m, IH), 3.47 (m, IH), 2.64-3.23 (m, 4H); ES-MS (m/z) 374 [M+Hf .
C. 2-Benzoyl-6-methoxy-l-{4-[(2-piperidyl)ethoxy]benzyl} -1,2,3,4- tetrahydroisoquinoline The title compound was prepared as described in Example 14.E, using 2- benzoyl-l-(4-hydroxybenzyl)-6-methoxy-l,2,3,4-tetrahydroisoquinoline (0.60 g, 1.6 mmol) to provide the title compound (0.521 g, 67% yield).
D. 2-Benzoyl-l-{4-[(2-piperidyl)ethoxy]benzyl}-l,2,3,4-tetrahydroisoquinoiin-6-ol Trifluoroacetate The title compound was prepared as described in Example 14.F, using 2- benzoyl-6-methoxy-l-{4-[(2-piperidyl)ethoxy]benzyl}-l,2,3,4-tetrahydroisoquinoline (0.50 g, 1.03 mmol) to provide the title compound (0.137 g, 28%) yield): 1H NMR (DMSO-d6) 9.5 (br, 2H), 7.3-7.41 (m, 2H), 7.08-7.23 (m, 4H), 6.82-6.95 (m, 3H), 6.51- 6.64 (m, 2H), 5.69 (m, IH), 4.59 (m, IH), 4.29 (t, 2H), 3.3-3.9 (m, 5H), 2.5-3.17 (m 7H), 1.6-1.9 (m, 4H), 1.39 ( , 2H); ES-MS (m/z) 471 [M+H]÷.
EXAMPLE 25
SYNTHESIS OF 2-(4-FLUOROBENZYL)- 1 - {4-[(2-PIPERIDYL)ETHOXY]BENZYL} -1,2,3,4-
TETRAHYDRθisoQUiNθLiN-6-θL TRIFLUOROACETATE
The title compound was prepared as described in Example 27. A, using 2-
(4-fluorobenzoyl)-l-{4-[(2-piperidyl)ethoxy]benzyl}-l,2,3,4-tetrahydroisoquinolin-6-ol (0.10 g, 0.205 mmol) to provide the title compound (0.054 g, 56% yield): 1H NMR (DMSO-d6) 10.0 (br, 2H), 7.32-7.75 (m, 4H), 6.95 (m, 4H), 6.66 (d, IH), 6.40 (dd, IH), 6.13 (dd, IH), 4.6 (m, IH), 4.43 (t, 2H), 2.6-3.9 (m, 10H), 2.0-1.4 (m, 10H); ES-MS (m/z) 475 [M+H]+.
EXAMPLE 26
SYNTHESIS OF 2-(4-FLUOROPHENΎL)-1-{4-NITROBENZYL}-1,2,3,4- TETRAHYDROISOQUINOLIN-6-OL
Reaction Scheme
Scheme for EExample 26, 46, 49 (Nitrogen-containing sidechain analogs)
Example 49
A. N- {4-FIuorophenyl} -2-(4-nitrophenyl)-N- {2-[3- (pheny lmethoxy)phenyl] ethyl } acetamide
The title compound was prepared as described in Example 12.E using 4- nitrophenylacetic acid (5.1g, 28 mmol) to provide the title compound (8.7g, 90% yield): ES-MS (m/z) 485 [M+H]+.
B. 2-(4-Fluorophenyl)-6-phenylmethoxy-l-(4-nitrobenzyl)- 1,2,3,4- tetrahydroisoquinoline
The title compound was prepared as described in Example 12.E using N-
{4-fluorophenyl}-2-(4-nitrophenyl)-N-{2-[3-(phenylmethoxy) phenyl]ethyl} acetamide (8.7 g, 18 mmol) to provide the title compound (3.5 g, 41.5% yield): ES-MS (m/z) 469
[M+H]+.
C. 2-(4-Fluorophenyl)-l-(4-nitrobenzyl)-l,2,3,4-tetrahydroisoquinolin-6-ol
The title compound was prepared as described in Example 3.D using 2- (4-fluorophenyl)-6-phenylmethoxy- 1 -(4-nitrobenzyl)- 1 ,2,3 ,4-tetrahydroisoquinoline (0.11 g, 0.23 mmol). Purification by column chromatography (Siθ2, hexanes/ethyl acetate, 2:1) provided the title compound (0.029 g, 33% yield): ES-MS (m/z) 379 [M+H]+.
EXAMPLE 27 SYNTHESIS OF 2-BENZYL- 1 - {4-[(2-PIPERIDYL)ETHOXY]BENZYL}-1 ,2,3,4- TETRAHYDROISOQUINOLIN-6-OL TRIFLUOROACETATE
A. 2-Benzyl-l-{4- (2-piperidyl)ethoxy]benzyl}-l,2,3,4-tetrahydroisoquinolin-6-ol Trifluoroacetate
To a solution of 2-Benzoyl-l-{4-[(2-piperidyl)ethoxy]benzyl}-l,2,3,4- tetrahydroisoquinolin-6-ol (0.1 g, 0.21 mmol) in tetrahydrofuran (10 mL) was added a solution of 1.0 M borane-tetrahydrofuran complex in tetrahydrofuran (0.21 mL, 0.21 mmol), and the reaction was heated at 80°C for 3-4 hours. After cooling to room temperature, a 5% hydrochloride solution was added, and the mixture was stirred for another hour. The reaction was then basified with a solution of saturated sodium bicarbonate and extracted with CH C12. The organic layer was dried over MgSO , filtered, and concentrated. The residue was purified by HPLC (C-18 column, 10-100%
acetonitrile/water with 0.1% trifluoroacetic acid) to provide the title compound (0.047 g, 48% yield): 1H NMR (CDC13) 11.2 (br, 2H), 7.41 (m, 3H), 6.80 (d, 2H), 6.70 (d, 2H), 6.6 (m, IH), 6.18 (m, 4H), 4.34 (m, IH), 4.17 (t, 2H), 3.92 (m, IH), 3.76 (m, 2H), 3.62 (m, 4H), 3.40 (m, IH), 3.01 (t, 2H), 2.00 (m, 4H), 1.88 (m, 4H), 1.75 (m, 2H); ES- MS (m/z) 457 [M+H]+.
EXAMPLE 28
SYNTHESIS OF 2-(2-CHLOROPYRIMIDIN-4-YL)-1 - {4-[(2-PIPERIDYL)ETHOXY]BENZYL}-
1 ,2,3,4-TETRAHYDROISOQUINOLIN-6-OL TRIFLUOROACETATE
Reaction Scheme
Scheme for Example 28
NaHCQ3
A. 2-(2-Chloropyrimidin-4-yl)-6-methoxy-l-[4-(phenylmethoxy)benzyl]-l,2,3,4- tetrahydroisoquinoline
A mixture of 6-methoxy-l-[4-(phenylmethoxy)benzyl]-l,2,3,4- tetrahydroisoquinoline (0.72 g, 2.0 mmol), 2,4-dichloropyrimidine (0.298 g, 2.0 mmol), and sodium bicarbonate (0.2 g, 2.4 mmol) in ethanol (10 mL) was heated at 80 °C for 3 hours. It was quenched with water and extracted with CH2C . The organic layer was dried over MgSO , filtered, and concentrated. The residue was purified by chromatography (Siθ2, 30-6-% ethyl acetate/hexane) to provide the title compound (0.749 g, 79% yield): 1H NMR (CDC13) 7.95 (d, IH), 7.32-7.41 (m, 4H), 6.94 (d, 2H), 6.83 (d, 2H), 6.69 (m, 3H), 6.37 (m, IH), 5.9 (d, IH), 5.03 (s, 2H), 4.97 (m, IH), 3.80 (s, 3H), 3.25-3.62 (m, 2H), 3.13 (m, IH), 2.86 (m, 3H); ES-MS (m/z) 472 [M+H]+.
B. 2-(2-Chloropyrimidin-4-yl)- 1 -(4-hydroxybenzyl)-6-methoxy- 1 ,2,3,4- tetrahydroisoquinoline
The title compound was prepared as described in Example 14.D, using 2-
(2-chloropyrimidin-4-yl)-6-methoxy-l-[4-(phenylmethoxy)benzyl]- 1,2,3,4- tetrahydroisoquinoline (0.70 g, 1.48 mmol) to provide the title compound (0.089 g, 16%> yield): Η NMR (CDC13) 7.91 (d, IH), 6.91 (m, 3H), 6.71 (m, 4H), 6.37 (m, IH), 5.85
(d, IH), 4.75 (dd, IH), 3.80 (s, 3H), 3.3-3.65 (m, 2H), 2.6-3.25 (m, 4H); ES-MS (m/z)
382 [M+H]+.
C. 2-(2-Chloropyrimidin-4-yl)-6-methoxy-l-{4- (2-piperidyl)ethoxy]benzyI}- 1 ,2,3,4-tetrahydroisoquinoline
The title compound was prepared as described in Example 14.E, using 2-
(2-chloropyrimidin-4-yl)-l-(4-hydroxybenzyπ-6-methoxy- 1,2,3,4- tetrahydroisoquinoline (0.089 g, 0.23 mmol) to provide the title compound (0.1 1 g, 97% yield): ES-MS (m/z) 493 [M+H]+. D. 2-(2-ChIoropyrimidin-4-yl)- 1 - { 4-[(2-piperidyl)ethoxylbenzyl } - 1 ,2,3,4- tetrahydroisoquinolin-6-ol Trifluoroacetate
The title compound was prepared as described in Example 14.F, using 2- (2-chloropyrimidin-4-yl)-6-methoxy-l-{4-[(2-piperidyl)ethoxy]benzyl} -1,2,3,4- tetrahydroisoquinoline (0.1 1 g, 0.22 mmol) to provide the title compound (0.84 g, 76% yield): 1H NMR (CDC13) 1 1.9 (br, 2H), 8.58 (d, IH), 8.1 (m, IH), 7.8 (m, IH), 7.06 (d, IH), 6.96 (m, IH), 6.87 (m, IH), 6.64-6.7 (m, 2H), 5.98 (m, IH), 5.00 (m, IH), 4.31 (t, 2H), 3.41-3.73 (4H), 2.81-3.14 (m, 4H), 2.04 (m, 4H), 1.92 (m, 4H), 1.87 (m, 2H); ES- MS (m/z) 479 [M+H]+.
EXAMPLE 29
SYNTHESIS OF 2-[(2-DLMETHYLAMINO)PYRIMIDIN-4-YL]-1-{4-[(2-
PIPERIDYL)ETHOXY]BENZYL}-1,2,3,4-TETRAHYDROISOQUINOLIN-6-OL
TRIFLUOROACETATE
Reaction Scheme
Scheme for Example 29
A solution of 2-(2-chloropyrimidin-4-yl)-6-methoxy-l-(4-
(phenylmethoxy)benzyl)-l,2,3,4-tetrahydroisoquinoline (from Example 28) in 40% dimethylamine/water (15 mL) in a sealed mbe was heated at 1 10 °C for 4 hours. The reaction was quenched with water and extracted with CH2CL. The organic layer was dried over MgSO4, filtered, and concentrated to provide the title compound (0.683 g,
96% yield): Η NMR (CDCI3) 7.91 (d, IH), 7.32-7.43 (m, 4H), 6.87 (d, 2H), 6.80 (d,
2H), 6.62-6.73 (m, 4H), 5.77 (d, IH), 5.02 (s, 2H), 3.78 (s, 3H), 3.52 (m, 2H), 3.19 (s, 6H), 3.12 (m, IH), 3.01 (m, 2H), 2.83 (m, IH), 2.70 (m, IH); ES-MS (m/z) 481
[M+Hf.
B. 2- [(2-Dimethylamino)pyrimidin-4-yl]- 1 -(4-hydroxybenzy i)-6-methoxy- 1 ,2,3,4- tetrahydroisoquinoline
The title compound was prepared as described in Example 14.D, using 2- [(2-dimethylamino)pyrimidin-4-yl]-6-methoxy- 1 - [4-(phenylmethoxy)benzy 1] - 1,2,3,4- tetrahydroisoquinoline (0.68 g, 1.4 mmol) to provide the title compound (0.351 g, 64% yield): Η NMR (CDC13) 7.82 (s, IH), 6.82 (m, 3H), 6.66 (m, 5H), 5.71 (d, IH), 3.78 (s,
3H), 3.51 (m, 2H), 3.17 (s, 6H), 2.66-3.21 (m, 5H); ES-MS (m/z) 391 [M+H]+.
C. 2-[(2-Dimethylamino)pyrimidin-4-yl]-6-methoxy- 1 - {4-[(2- piperidyl)ethoxy]benzyl}-1.2.3,4-tetrahydroisoquinoline
The title compound was prepared as described in Example 14.E, using 2- [(2-dimethylamino)pyrimidin-4-yl]-l-(4-hydroxybenzyl)-6-methoxy-l,2,3,4- tetrahydroisoquinoline (0.3 g, 0.77 mmol) to provide the title compound (0.298 g, 77% yield): Η NMR (CDC13) 7.91 (d, IH), 7.86 (d, 2H), 6.70-6.74 (m, 3H), 6.61-6.65 (m, 2H), 5.77 (d, IH), 4.06 (t, 2H), 3.78 (s, 3H), 3.51 (m, 2H), 3.51 (m, IH), 3.18 (s, 6H), 3.02 (m, IH), 2.76 (t, 2H), 2.61-2.86 (m, 3H), 2.51 (m, 4H), 1.62 (m, 4H), 1.45 (m, 2H); ES-MS (m/z) 502 [M+H]+.
D. 2-[(2-Dimethylamino)pyrimidin-4-yl]-l-{4-[(2-piperidyl)ethoxy]benzyl}- 1 ,2,3,4-tetrahydroisoquinolin-6-ol Trifluoroacetate The title compound was prepared as described in Example 14.F, using 2-
[(2-dimethylamino)pyrimidin-4-yl]-6-methoxy-l-{4-[(2-piperidyl)ethoxy]benzyl}- 1,2,3,4-tetrahydroisoquinoline (0.295 g, 0.59 mmol) to provide the title compound
(0.121 g, 42% yield): 1H NMR (CDC13) 11.7 (br, 2H), 7.83 (d, IH), 7.45 (d, IH), 6.89- 6.96 (m, 2H), 6.65-6.80 (m, 4H), 5.35 (d, IH), 4.31 (t, 2H), 3.63-3.69 (m, 3H), 3.43- 3.58 (m, 4H), 3.24 (s, 3H), 3.21 (s, 3H), 3.02 (t, 2H), 2.82 (m, 4H), 1.91 (m, 4H), 1.87 (m, 2H); ES-MS (m/z) 488 [M+H]+.
EXAMPLE 30
SYNTHESIS OF 1-[(4-HYDROXYPHENYL)METHYL]-2-[4-(MORPHOLIN-4-
YLACETAMIDO)PHENYL]-1 ,2,3,4-TETRAHYDROISOQUINΌLIN-6-OL
A. 6-Methoxy-2-(4-nitrophenyl)-l-[4-(phenylmethoxy benzyl]-l,2,3,4- tetrahydroisoquinoline
A solution of 6-methoxy-l-[4-(phenylmethoxy)benzyl]-l,2,3,4- tetrahydroisoquinoline (2.10 g, 5.84 mmol) and l-fluoro-4-nitrobenzene (1.65 g, 11.7 mmol) in 40 mL of DMSO was treated with powdered K2CO3 (1.62 g, 11.7 mmol) and the reaction mixture was warmed at 120°C for 12 h. The reaction mixture was cooled to room temperature and 300 mL of water was added. The aqueous layer was extracted with CH2O2 and the combined organic layer was washed with water, dried over MgSO , then concentrated under reduced pressure. The crude product was purified by flash chromatography to provide the title compound (2.50 g, 89%>). ES-MS, (m/z) 481 [M+H]+. B. 2-(4-Aminophenyl)-6-methoxy-l-[4-(phenylmethoxy)benzyl]-l, 2,3,4- tetrahydroisoquinoline
A suspension of 6-methoxy-2-(4-nitrophenyl)-l-[4-
(phenylmethoxy)benzyl]-l,2,3,4-tetrahydroisoquinoline (0.70 g, 1.46 mmol) and
SnCl2*H2O (1.35 g, 6.0 mmol) in 20 mL of THF/HOAc (1 :1) and 3 mL of water was heated at 60 °C for 3 h. The reaction mixture was concentrated under reduced pressure
and the resulting residue was quenched by the addition of saturated aqueous NaHCO3 (50 mL). The aqueous layer was extracted with EtOAc (3 x 50 mL) and the combined organic layer was dried over MgSO then concentrated. The crude product was purified by flash chromatography to provide the title compound (0.63 g, 95%> yield). ES-MS, (m/z) 451 [M+H]+.
C. 6-Methoxy-2-[4-(morpholin-4-ylacetamide)phenyl]- 1 -[4- (phenylmethoxy)benzyl]-l,2,3,4-tetrahydroisoquinoline
A solution of 2-(4-aminophenyl)-6-methoxy-l-[4-
(phenylmethoxy)benzyl]-l,2,3,4-tetrahydroisoquinoline (0.225 g, 0.50 mmol) and TEA (0.061 g, 0.6 mmol) in 3 mL of CH2CI2 at 0°C was treated with bromoacetyl bromide (0.121 g, 0.60 mmol) in 1 mL of CH2CI2. After 30 minutes, excess morpholine was added (0.20 mL) and the reaction mixture was warmed to room temperature and stirred overnight. The reaction was quenched by the addition of saturated aqueous NaHCO3 (0.5 mL) and the aqueous layer was extracted with CH;C (4 x 2 mL). The combined organic layer was dried over MgSO and concentrated. The crude product was purified by flash chromatography to provide the title compound (0.263 g, 91% yield). ES-MS, (m/z) 578 [M+H]+.
D. l-[4-(hydroxyphenyl)methyl]-6-methoxy-2-[4-(morpholin-4- ylacetamide)phenyl]-l,2,3,4-tetrahydroisoquinoline A solution of 6-methoxy-2-[4-(morpholin-4-ylacetamide)phenyl]-l-[4-
(phenylmethoxy)phenylmethyl]-l,2,3,4-tetrahydroisoquinoline (0.24 g, 0.42 mmol) in 2 mL of EtOH/THF (1 :1) was degassed and placed under a H2 atmosphere. Palladium (10%o wt. on activated carbon, 0.050 g) in 0.5 mL of EtOH was introduced and the reaction mixture was stirred overnight. The mixture was filtered through celite and the filter cake was rinsed with CH2CI2. The solution was concentrated and the crude product purified by column chromatography to provide the title compound (0.18 g, 89% yield). ES-MS, (m/z) 488 [M+H]+.
E. l-(4-Hydroxybenzyl)-2-[4-(mo holin-4-ylacetamido)phenyl]-l ,2,3,4- tetrahydroisoquinolin-6-ol A solution of l-(4-hydroxybenzyl)-6-methoxy-2-[4-(morpholin-4- ylacetamide)phenyl]-l,2,3,4-tetrahydroisoquinoline (0.060 g, 0.123 mmol) in 1 mL of
CH2C12 at 0°C was treated with BBr3 (1M in CH2C12, 0.5 mL, 0.5 mmol). The reaction mixture was stirred for 1 hour at 0 °C then it was quenched by the addition of saturated aqueous NaHCO3 (2 mL). The aqueous layer was extracted with CH2C12 (4 x 2 mL) and the combined organic layer was dried over MgSO then concentrated. The crude product was purified by column chromatography to provide the title compound (0.035 g, 60% yield). ES-MS, (m/z) 474 [M+Hf.
EXAMPLE 31
SYNTHESIS OF 2-(4-ACETAMIDOPHENYL)-1 -(4-HYDROXYBENZYL)- 1 ,2,3,4-
TETRAHYDROISOQUINOLIN-6-OL
A. 2-(4-Acetamidophenyl)-6-methoxy-l-[4-(phenylmethoxy)benzyl]- 1,2,3,4- tetrahydroisoquinoline
A solution of 2-(4-aminophenyl)-6-methoxy-l-[4-
(phenylmethoxy)benzyl]-l,2,3,4-tetrahydroisoquinoline (0.205 g, 0.46 mmol) and TEA (0.060 g, 0.6 mmol) in 1 mL of CH2C12 at 0 °C was treated with acetyl chloride (0.043 g, 0.55 mmol). The reaction mixture was warmed to room temperature and stirred for 3 hours. The reaction was quenched by the addition of saturated aqueous NaHCO3 (0.5 mL). The organic layer was separated and the aqueous layer was extracted with CH2CI2 (3 x 2 mL). The combined organic layer was dried over MgSO4 then concentrated. The crude product was purified by column chromatography to provide the title compound (0.195 g, 87% yield). ES-MS, (m/z) 493 [M+H]+.
B. 2-(4-Acetamidophenyl)-l -(4-hydroxybenzyl)-6-methoxy-l, 2,3,4- tetrahydroisoquinoline
A solution of 2-(4-acetamidophenyl)-6-methoxy-l-[4- (phenylmethoxy)benzyl]- 1,2, 3, -tetrahydroisoquinoline (0.190 g, 0.386 mmol) in 2 mL
of EtOH/THF (1 :1) was debenzylated with 10% Pd/C under an H2 atmosphere as described in Example 30. F to provide the title compound (0.148 g, 95% yield): ES-MS (m/z) 403 [M+H]+.
C. 2-(4-Acetamidophenyl)-l-(4-hydroxybenzyl)-l,2,3,4-tetr.ahydroisoquinolin-6-ol A solution of 2-(4-acetamidophenyl)-l-(4-hydroxybenzyl)-6-methoxy-
1,2,3,4-tetrahydroisoquinoline (0.025 g, 0.062 mmol) in 1 mL of CH2CI2 was demethylated with BBr3 as described in Example 30. G to provide the title compound (0.018 g, 75% yield). ES-MS, (m/z) 389 [M+H]+.
EXAMPLE 32 SYNTHESIS OF 2-(4-ACETAMIDOPHENYL)- 1 - {[4-(2-PIPERIDYLETHOXY)PHENYL]METHYL} -
1 ,2,3,4-TETRAHYDROISOQUINOLIN-6-OL
A. 2-(4- Acetamidophenyl)-6-methoxy- 1 - { [4-(2-piperidyl)ethoxy]benzyl } - 1 ,2 ,3 ,4- tetrahydroisoquinoline A solution of 2-(4-acetamidophenyl)-l-(4-hydroxybenzyl)-l,2,3,4- tetrahydroisoquinolin-6-ol (0.120 g, 0.298 mmol) in 2 mL of DMF was O-alkylated with l-(2-chloroethyl)piperidine monohydrochloride and K2CO3 as described in
Example 3.D to provide the title compound (0.102 g, 67% yield): ES-MS, (m/z) 514
[M+H]+. B. 2-(4- Acetamidophenyl)- 1 - { [4-(2-piperidyl)ethoxy]benzyl } - 1 ,2,3 ,4- tetrahydroisoquinolin-6-ol
A solution of N-[4-(6-methoxy-l-{[4-(2-piperidyl)ethoxy]benzyl}-2- l,2,3,4-tetrahydroisoquinolyl)phenyl]acetamide (0.102 g, 0.199 mmol) was demethylated with BBr3 in CH2CI2 as described in Example 30. G to provide the title compound (0.062 g, 62%). ES-MS, (m/z) 500 [M+Hf.
EXAMPLE 33 SYNTHESIS OF 2-[4-(MORPHOLIN-4-YLACETAMIDO)PHENYL]- 1 -{[4-(2- PIPERIDYL)ETHOXY]BENZYL}-1 ,2,3,4-TETRAHYDROISOQUINOLIN-6-OL
A. 6-Methoxy-2-[4-(morpholin-4-ylacetamido)phenyl]-l-{[4-(2- piperidyl)ethoxy]benzyl} - 1 ,2,3,4-tetrahydroisoquinoline
A suspension of N-(4-{l-[(4-hydroxyphenyl)methyl]-6-methoxy-2-
(l,2,3,4-tetrahydro-isoquinolyl)}-phenyl)-2-moφholin-4-ylacetamide (0.120 g, 0.246 mmol), K2CO3 (0.086 g, 0.62 mmol), and l-(2-chloroethyl)piperidine monohydrochloride (0.052 g, 0.28 mmol) in 1 mL of DMF was warmed at 90 °C for 8 hours. The solvent was removed under vacuum and the residue was suspended in 10 mL of CH2Cl2/MeOH (5:1). The resulting suspension was filtered through celite and the filtrate was concentrated. The crude product was purified by flash chromatography to provide the title compound (0.121 g, 82% yield). ES-MS, (m/z) 599 [M+H]+. B. 2-[4-(Morpholin-4-ylacetamido)phenyl]- 1 - { 4-(2-piperidyl)ethoxy]benzyl } - l,2,3,4-tetrahydroisoquinolin-6-ol
A solution of 6-methoxy-2-[4-(morpholin-4-ylacetamido)phenyl]-l-{[4-
(2-piperidyl)ethoxy]benzyl}-l,2,3,4-tetrahydroisoquinoline (0.080 g, 0.134 mmol) in 1 mL of CH2CI2 was demethylated with BBr3 as described in Example 30. G to provide the title compound after flash chromatography (0.038 g, 48% yield): ES-MS, (m/z) 585
[M+H]+.
EXAMPLE 34
SYNTHESIS OF 2-(NAPHTHYL)-1-{4-[(2-PIPERIDYL)ETHOXY]BENZYL}-1,2,3,4- TETRAHYDROISOQUINOLIN-6-OL
Reaction Scheme
Scheme for Examples 34, 36, 38, 39 and 43
A mixture of methyl 4-hydroxyphenylacetate (4.985 g, 30 mmol), 2- chloroethylpiperidine hydrochloride (6.624 g, 36 mmol), and potassium carbonate (10.35 g, 75 mmol) in dimethylformamide (30 mL) was heated at 80°C overnight. After cooling to room temperature, the mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO4, filtered, and concentrated. The residue was dissolved in methanol (30 mL) and 5 N sodium hydroxide (15 mL) then heated at 90 °C for 1.5 hour. Methanol was evaporated and the basic solution was acidified with 6 N hydrochloride solution. Water was evaporated, and the residue was extracted with methanol and concentrated. The residue was then extracted with CH2CI2 and concentrated to provide the title compound (6.002 g, 76% yield): Η NMR (CDCI3) 12.04 (br, IH), 7.19 (d, 2H), 6.82 (d, 2H), 4.49 (m, IH), 3.38-3.67 (m 5H), 2.83 (m, 4H), 2.22 (m, 2H), ( 1.87 (m, 3H), 1.42 (m, IH); ES- MS (m/z) 264 [M+H]+. B. 2-(3-Hydroxyphenyl)-N-naphthylacetamide
To a solution of 3-hydroxyphenylacetic acid (3.04 g, 20 mmol) in dimethylformamide (30 mL) and 1 -hydroxybenzotriazole (3.24 g, 24 mmol) at 0 °C under nitrogen was added l-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (4.60 g, 24 mmol). After 30 minutes, 1 -aminonaphthyline (2.86 g, 20 mmol) was added, and the mixture was stirred overnight at room temperature. The reaction was quenched with 5%> hydrochloride and extracted with ethyl acetate. The organic layer was washed with a 10% sodium carbonate solution, washed with brine, dried over MgSO4, filtered, and concentrated to provide the title compound (5.239 g, 94% yield): Η NMR (DMSO-d6) 9.66 (br, IH), 9.04 (s, 1H),7.96 (dd, IH), 7.85 (dd, IH), 7.74 (dd, IH), 7.68 (d, IH), 7.18-7.49 (m, 3H), 7.16 (t, IH), 6.92 (m 2H). 6.73 (d, IH), 3.76 (s, 2H); ES-MS (m/z) 278 [M+H]+.
C. N-Naphthyl-2-[3-(phenylmethoxy)phenyl]acetamide
A mixture of 2-(3-hydroxyphenyl)-N-naphthylacetamide (5.00 g, 18.03 mmol), benzyl bromide (3.76 g, 22.0 mmol), and potassium carbonate (4.14 g, 30.0 mmol) in acetone (50 mL) was heated to reflux overnight. The reaction was quenched with water and extracted with ethyl acetate. The organic layer was dried over MgSO ,
filtered, and concentrated to provide the title compound (3.176g, 48%o yield): Η NMR (DMSO-dή) 10.13 (br, IH), 8.06 (m, 1H),7.94 (m, IH), 7.77 (d. IH), 7.67 (d, IH), 7.26- 7.56 (m, 9H), 6.92-7.11 (m, 3H), 5.11 (s, 2H), 3.79 (s, 2H); ES-MS (m/z) 368 [M+Hf.
D. Naphthyl {2-[3-(phenylmethoxy)phenyl]ethyl} amine To a solution of N-naphthyl-2-[3-(phenylmethoxy)phenyl]acetamide
(3.00 g, 8.16 mmol) in tetrahydrofuran (25 mL) under nitrogen was added a solution of 1.0 M borane-tetrahydrofur.an complex in tetrahydrofuran (12.3 mL, 12.3 mmol) and heated to reflux for 5 hours. The reaction was quenched with a 5% hydrochloride solution. After stirring 30 minutes, the reaction was basified with a 10% sodium carbonate solution and extracted with CH2CI2. The organic layer was dried over MgSO4, filtered, and concentrated to provide the title compound (2.724 g, 94% yield): 1H NMR (CDC13) 7.78 (d, IH), 7.67 (d, IH), 7.18-7.46 (m, 10H), 6.89 (m, 3H), 6.66 (d, IH), 5.01 (s, 2H), 4.40 (br, IH), 3.55 (t, 2H), 3.05 (t, 2H); ES-MS (m/z) 354 [M+H]+.
E. 2-Naphthyl-6-(phenylmethoxy)- 1 - {4-[(2-piρeridyl)ethoxy]benzyl } - 1 ,2,3,4- tetrahydroisoquinoline
To a solution of naphthyl {2-[3-(phenylmethoxy)phenyl]ethyl} amine (0.42 g, 1.19 mmol) and 2- {[4-(2-piperidyl)ethoxy]phenyl} acetic acid (0.316 g, 1.20 mmol) in chlorobenzene (6 mL) under nitrogen was added a solution of 2.0 M phosphorus trichloride in CH2CI2 (0.6 mL, 1.2 mmol), The reaction was heated at 140 °C for 12 hours. After cooling to room temperature, the solvent was evaporated. Methanol and ethyl acetate were added and concentrated several times to provide a residue (0.508 g).
The residue was dissolved in acetonitrile (8 mL) and phosphorus oxychloride (2 mL), and then heated at 80°C for 16 hours. After cooling to room temperature, the solvents were evaporated. Ethyl acetate was added and evaporated several times. The residue was dissolved in methanol (10 mL) and sodium borohydride (0.6 g, 15.8 mmol) was added in small portions. After stirring at room temperature overnight, the reaction was quenched with a solution of saturated sodium bicarbonate and extracted with ethyl acetate. The organic layer was dried over MgSO , filtered, and concentrated. The residue was purified by chromatography (SiO2, 0-10% methanol/CH2Cl2) to provide the title compound (0.217 g, 31% yield): Η NMR
(CDCI3) 8.06 (d, IH), 7.79 (d, IH), 7.33-7.51 (m, 8H), 7.20 (m, IH), 6.68-6.96 (m, 8H), 5.06 (s, 2H), 4.66 (t, IH), 4.11 (m, IH), 4.01 (t, 2H), 3.76 (m, IH), 3.45 (dd, IH), 3.18 (m IH), 2.90 (dd, IH), 2.69-2.78 (m and t, 3H), 2.48 (m, 4H), 1.59 (m, 4H), 1.43 (m, 2H); ES-MS (m/z) 483 [M+H]+. F. 2 -Naphthyl- l-{4- (2-piperidyl)ethoxy]benzyl}-l,2,3,4-tetrahydroisoquinolin-6- ol
The title compound was prepared as described in Example 14.D, using 2- naphthyl-6-(phenylmethoxy)-l-{4-[(2-piperidyl)ethoxy]benzyl}-l,2,3,4- tetrahydroisoquinoline (0.21 g, 0.36 mmol) to provide the title compound (0.127 g, 72% yield): ): Η NMR (CDCI3) 8.04 (d, IH), 7.78 (d, IH), 7.37-7.47 (m, 4H), 7.22 (m, IH),
6.92 (m, 3H), 6.54-6.91 (m, 5H), 4.61 (t, IH), 4.02 (t, 2H), 3.60-3.79 (m, 3H), 3.37 (m,
IH), 3.16 (m IH), 2.93 (m, IH), 2.74 (t, 2H), 2.52 (m, 4H), 1.61 (m, 4H), 1.44 (m, 2H);
ES-MS (m/z) 493 [M+H]+.
EXAMPLE 35 SYNTHESIS OF 2-[(4-FLUORO-2-METHYL)PHENYL]- 1 - {4-[(2-
PIPERID YL)ETHOXY]BENZYL} - 1 ,2,3 ,4-TETRAH YDROISOQUTNOLIN-6-OL
A. 2-(3-Hydroxyphenyl)-N-[ (4-fluoro-2-methyl)phenyl]acetamide
The title compound was prepared as described in Example 34.B using 2- methyl-4-fluoro aniline (2.5 g, 20 mmol) to provide the title compound (4.2 g, 81% yield): ES-MS (m/z) 260 [M+Hf .
B. 2-[3-(Phenylmethoxy)phenyl]-N-[(4-fluoro-2-methyl) phenyl] acetamide
The title compound was prepared as described in Example 34. C using 2- (3-hydroxyphenyl)-N-[(4-fluoro-2-methyl) phenyl] acetamide (4 g, 15.4 mmol) to provide the title compound (4.4 g, 82% yield): ES-MS (m/z) 350 [M+H]+. C. {2-[3-(Phenylmethoxy)phenyl]ethyl}[4-fluoro-2-methylphenyl]amine
The title compound was prepared as described in Example 34. D using 2- [3-(phenylmethoxy)phenyl]-N-[(4-fluoro-2-methyl)phenyl]acetamide (4.3 g, 12.3 mmol) to provide the title compound (3.47 g, 84%, yield): ES-MS (m/z) 336 [M+H]+.
D. N-{(4-Fluoro-2-methyl)phenyl|-2-(4-hydroxyphenyl)-N-[2-{3- (phenylmethoxy)phenyl } ethyl] acetamide
The title compound was prepared as described in Example 34. B from {2-
[3-(phenylmethoxy)phenyl]ethyl}[4-fluoro-2-methylphenyl]amine (1 g, 3 mmol) to provide the title compound (0.7 g, 50% yield): ES-MS (m z) 470 [M+H]+.
E. 2-[(4-Fluoro-2-methyl)phenyl]-6-phenylmethoxy-l-(4-hydroxybenzyl)-l, 2,3,4- tetrahydroisoquinoline
The title compound was prepared as described in Example 1.D using N-
{(4-fluoro-2-methyl)phenyl}-2-(4-hydroxyphenyl)-N-[2-{3-(phenylmethoxy) phenyl} ethyl] acetamide (0.7 g., 1.5 mmol). Purification by column chromatography
(Siθ2, ethylacetate/hexanes, 5:1) provided the title compound (0.124 g, 18%> yield): ES- MS (m/z) 454 [M+H]+.
F. 2-[(4-Fluoro-2-methyl)phenyl]-6-phenylmethoxy-l-{4- (2-piperidyl)ethoxy] benzyl}-!, 2, 3,4-tetrahydroisoquinoline
The title compound was prepared as described in Example 3.D from 2-
[(4-fluoro-2-methyl)phenyl]-6-phenylmethoxy-l-(4-hydroxybenzyl)-l, 2,3,4- tetrahydroisoquinoline (0.124 g, 0.27 mmol) to provide the title compound (0.12 g, 80% yield): ES-MS (m/z) 565 [M+H]+.
G. 2-[(4-Fluoro-2-methyl)phenyl1-l-{4- (2-piperidyl)ethoxy]benzyl} -1,2,3,4- tetrahydroisoquinolin-6-ol
The title compound was prepared as described in Example 14.D using 2- [(4-fluoro-2-methyl]phenyl)-6-phenylmethoxy-l-{4-[(2-piperidyl)ethoxy]benzyl}-
1,2, 3,4-tetrahydroisoquinoline (0.12 g, 0.2 mol) to provide the title compound (0.1 g,
77% yield): ES-MS (m/z) 475 [M-t-Hf.
EXAMPLE 36
SYNTHESIS OF 1 - {4-[(2-PIPERIDYL)ETHOXY]BENZYL}-2-[(4-
TRIFLUOROMETHYL)PHENYL]-1 ,2,3,4-TΈTRAHYDROISOQUINOLΓN-6-OL
A. 2-(3-Hydroxyphenyl)-N-[4-(trifluoromethyl)phenyl]acetamide
The title compound was prepared as described in Example 34.B, using 4- (trifluoromethyl)aniline (1.61 g, 10.0 mmol) to provide the title compound (2.67 g, 90%> yield): ES-MS (m/z) 296 [M+H]+.
B. 2-[3-(Phenylmethoxy)phenyl]-N-[4-(trifluoromethyl)phenyl]acetamide The title compound was prepared as described in Example 34. C, using 2-
(3-hydroxyphenyl)-N-[4-(trifluoromethyl)phenyl]acetamide (2.10 g, 7.1 1 mmol) to provide the title compound (2.104 g, 77% yield): 1H NMR (CDC13) 7.52 (s, 5H), 7.31- 7.44 (m, 5H), 7.23 (br, IH), 6.95 (m, 3H), 5.09 (s, 2H), 3.73 (s, 2H); ES-MS (m/z) 386 [M+Hf. C. {2-[3-(Phenylmethoxy)phenyllethyl} [4-(trifluoromethyl)phenyl]amine
The title compound was prepared as described in Example 34. D, using 2- [3-(phenylmethoxy)phenyl]-N-[4-(trifluoromethyl)phenyl]acetamide (2.0 g, 5.19 mmol) to provide the title compound (1.745 g, 91% yield): Η NMR (CDCI3) 7.33-7.45 (m, 6H), 7.23-7.28 (m, IH), 6.81-6.88 (m, 3H), 6.59 (d, 2H), 5.06 (s, 2H), 4.00 (t, IH), 4.42 (m, 2H), 2.89 (t, 2H); ES-MS (m/z) 372 [M+Hf.
D. 6-(Phenylmethoxy)-l-{4-[(2-piperidyl)ethoxy]benzyl}-2-[4- (trifluoromethyl)phenyl]- 1 ,2, 3,4-tetrahydroisoquinoline
The title compound was prepared as described in Example 34. E, using
{2-[3-(phenylmethoxy)phenyl]ethyl} [4-(trifluoromethyl)phenyl]amine (0.55 g, 1.48 mmol) to provide the title compound (0.317 g, 36% yield): 1H NMR (CDCI3) 7.40-7.45
(m, 6H), 6.71-6.88 (m, 9H), 6.63 (dd, IH), 5.04 (s, 2H), 4.83 (t, IH), 4.83 (m, 3H), 3.60
(m, IH), 3.49 (m, IH), 3.13 (dd, IH), 2.91 (m, IH), 2.74 (m and t, 3H), 2.51 (m, 4H), 1.61 (m, 4H), 1.45 (m, 2H); ES-MS (m/z) 601 [M+H]+.
E. l-{4-[(2-Piperidyl)ethoxy]benzyl}-2-r4-(trifluoromethyl)phenyn-l,2,3.4- tetrahydroisoquinolin-6-ol The title compound was prepared as described in Example 14.D, using 6-
(phenylmethoxy)-l-{4-[(2-piperidyl)ethoxy]benzyl}-2-[4-(trifluoromethyl)phenyl]-
1,2,3,4-tetrahydroisoquinoline (0.30 g, 0.5 mmol) to provide the title compound (0.231 g, 91% yield): Η NMR (CDC13) 7.45 (d, 2H), 6.81 (m, 4H), 6.51-6.73 (m, 6H), 4.79
(dd, IH), 4.08 (t, 2H), 3.56 (m, IH), 3.43 (m, IH), 3.09 (dd, IH), 2.77-2.94 (m, 4H), 2.66 (m, IH), 2.61 (m, 4H), 1.64 (m, 4H), 1.46 (m, 2H); ES-MS (m/z) 511 [M+Hf.
EXAMPLE 37
SYNTHESIS OF 2-(4-CHLOROPHENYL)-1 -BENZYL- 1,2,3, 4-
TETRAHYDROISOQUTNOLIN-6-OL
A. 3-{2-[(4-Chlorophenyl)amino]ethyl}phenol
The title compound was prepared as described in Example 34. D, using N-(4-chlorophenyl)-2-(3-hydroxyphenyl)acetamide (2.0 g, 7.64 mmol) to provide the title compound (1.569 g, 83% yield): 1H NMR (CDC13) 7.19 (dd, IH), 7.10-7.14 (m, 2H), 6.78 (m, IH), 6.69-6.73 (m, 2H), 6.50-6.55 (m, 2H), 3.66 (br, IH), 3.36 (t, 2H), 2.86 (t, 2H), 2.05 (s, IH); ES-MS (m/z) 248 [M+H]+.
B. 2-(4-Chlorophenyl)-l-benzyl-l,2,3,4-tetrahydroisoquinoIin-6-ol
To a solution of 3-{2-[(4-chlorophenyl)amino]ethyl}phenol (0.20 g, 0.8 mmol) and phenylacetaldehyde (0.194 g, 1.6 mmol) in CH2Cl2 (6 mL) was added trifluoroacetic acid (0.148 g, 1.6 mmol). After stirring at room temperature overnight, the reaction was quenched with saturated sodium bicarbonate and extracted with
CH2C12. The organic layer was dried over MgSO4, filtered, and concentrated. The residue was purified by chromatography (SiO2, 15-30% ethyl acetate/hexane) to provide the title compound (0.203 g, 72% yield): Η NMR (CDC13) 7.19-7.24 (m, 4H), 7.16 (m, IH), 7.14 (m, IH), 6.70 (m, 2H), 6.71 (m, 2H), 6.61 (m, 2H), 6.54 (dd, IH), 4.77 (t, IH), 3.58 (ddd, IH), 3.47 (ddd, IH), 3.17 (dd, IH), 2.86-2.99 (m, 2H), 2.67 (m, IH); ES-MS (m/z) 350 [M+H]+.
EXAMPLE 38 SYNTHESIS OF 2-(3-FLUOROPHENYL)-1 - {4-[(2-PIPEPJDYL)ETHOXY]BENZYL}-1 ,2,3,4-
TETRAHYDROISOQUINOLIN-6-OL
A. N-(3-Fluorophenyl)-2-(3-hydroxyphenyl)acetamide
The title compound was prepared as described in Example 34.B, using 3- fluoroaniline (1.11 g, 10.0 mmol) to provide the title compound (2.339 g, 95% yield):
Η NMR (CDC13) 7.42 (dt, IH), 7.30 (d, IH), 7.21 (dd, IH), 7.12 (br, IH), 7.02 (dd, IH), 6.89 (d, IH), 6.77-6.83 (m, 3H), 5.09 (s, IH), 3.69 (s, 2H); ES-MS (m/z) 246
[M+H]+.
B. N-(3-Fluorophenyl)-2-[3-(phenylmethoxy)phenyl]acetamide
The title compound was prepared as described in Example 34. C, N-(3- fluorophenyl)-2-(3-hydroxyphenyl)acetamide (2.20 g, 8.97 mmol) to provide the title compound (2.639 g, 88% yield): ES-MS (m/z) 336 [M+H]+.
C. (3 -Fluorophenyl) {2-[3-(phenylmethoxy)phenyl]ethyl} amine
The title compound was prepared as described in Example 34. D, using N-(3-fluorophenyl)-2-[3-(phenylmethoxy)phenyl]acetamide (2.50 g, 7.45 mmol) to provide the title compound (1.441 g, 60% yield): ES-MS (m/z) 322 [M+H]+.
D. 2-(3-Fluorophenyl)-6-(phenylmethoxy)-l-{4-[(2-piperidyl)ethoxy]benzyl}- 1 ,2,3,4-tetrahydroisoquinoline
The title compound was prepared as described in Example 34.E, using
(3-fluorophenyl){2-[3-(phenylmethoxy)phenyl]ethyl} amine (0.642 g, 2.0 mmol) to provide the title compound (0.297 g, 27% yield): ES-MS (m/z) 551 [M+H]+.
E. 2-(3-Fluorophenyl)-l-{4-[(2-piperidyl)ethoxy]benzyl}-l,2,3,4- tetrahydroisoquinolin-6-ol
The title compound was prepared as described in Example 14.D, using 2-
(3-fluorophenyl)-6-(phenylmethoxy)-l-{4-[(2-piperidyl)ethoxy]beazyl}-l,2,3,4- tetrahydroisoquinoline (0.29 g, 0.53 mmol) to provide the title compound (0.187 g, 77% yield): ): 1H NMR (CDC13) 7.18 (dd, IH), 6.83 (m, 2H), 6.72 (d, 2H), 6.37-6.66 (m,
7H), 4.72 (dd, IH), 4.10 (t, 2H), 3.39-3.70 (m, 3H), 3.11 (dd, IH), 2.80-2.92 (m, 4H),
2.60-2.70 (m, 4H), 1.66 (m, 4H), 1.48 (m, 2H); ES-MS (m/z) 461 [M+H]+.
EXAMPLE 39 SYNTHESIS OF 2-(4-METHOXYPHENYL)- 1 - {4-[(2-PIPERIDYL)ETHOXY]BENZYL}-1,2,3,4-
TETRAHYDROISOQUINOLIN-6-OL
A. 2-(3-Hydroxyphenyl)-N-(4-methoxyphenyl)acetamide
The title compound was prepared as described in Example 34.B, using p- anisidine (1.23 g, 10.0 mmol) to provide the title compound (2.307 g, 90% yield): 1H NMR (CDCI3) 7.32 (d, IH), 7.30 (s, IH), 6.98 (br, IH), 6.94 (d, IH), 6.81 (m, 5H). 5.14 (s, IH), 3.71 (s, 3H), 3.68 (s, 2H); ES-MS (m/z) 258 [M+H]+.
B. N-(4-Methoxyphenyl)-2-[3-(phenylmethoxy)phenyl]acetamide
The title compound was prepared as described in Example 34. C, using 2- (3-hydroxyphenyl)-N-(4-methoxyphenyl)acetamide (2.20 g, 8.55 mmol) to provide the title compound (2.485 g, 84% yield): ES-MS (m/z) 348 [M+H]+. C. (4-Methoxyphenyl) {2-[3-(phenylmethoxy)phenyl]ethyl} amine
The title compound was prepared as described in Example 34. D, using N-(4-methoxyphenyl)-2-[3-(phenylmethoxy)phenyl]acetamide (2.1 g, 6.04 mmol) to provide the title compound (1.237 g, 61% yield): ES-MS (m/z) 334 [M+H]+.
D. 2-(4-Methoxyphenyl)-6-(phenylmethoxy)-l-{4-[(2-piperidyl)ethoxy]benzyl}- 1,2,3,4-tetrahydroisoquinoline
The title compound was prepared as described in Example 34. E, using
(4-methoxyphenyl){2-[3-(phenylmethoxy)phenyl]ethyl} amine (0.666 g, 2.0 mmol) to provide the title compound (0.311 g, 28% yield): ES-MS (m/z) 563 [M+H]+.
E. 2-(4-Methoxyphenyl)- 1 - {4-[(2-piperidyl)ethoxy]benzyl } - 1 ,2,3 ,4- tetrahydroisoquinolin-6-ol
The title compound was prepared as described in Example 14.D, using 2- (4-methoxyphenyl)-6-(phenylmethoxy)-l-{4-[(2-piperidyl)ethoxy]benzyl}- 1,2,3,4- tetrahydroisoquinoline (0.31 g, 0.55 mmol) to provide the title compound (0.238 g, 92%> yield): ): 1H NMR (CDC13) 6.81-6.89 (m, 6H), 6.69 (m, 2H), 6.61 (m, 2H), 6.51 (m, 2H), 4.64 (t, 1H),4.15 (t, 2H), 3.75 (s, 3H), 3.39-3.56 (m, 4H), 3.01-3.13 (t and m, 3H), 2.81 (m, 4H), 2.62 (m, IH), 1.74 (m, 4H), 1.52 (m, 2H); ES-MS (m/z) 473 [M+H]+.
EXAMPLE 40
SYNTHESIS OF 2-(4-FLUOROPHENYL)-6-METHOXΎ-1- {3-METHYL-4-[(2-
PIPERIDYL)ETHOXY]BENZYL}-1 ,2,3,4-TETRAHYDROISOQUINOLINE
A. 4-Hydroxy-3 -methyl-phenylacetic acid
To a solution of 3-methyl-4-methoxyphenylacetic acid (2.3 g., 12.8 mmol) in anh CH2CI2, cooled to 0°C, was added 15 ml of a solution of BBr3 (1.0 M in CH2C12) via syringe. After addition was complete, the reaction was allowed to warm to room temperature and then quenched with 5 ml water. The CH2CI2 was removed and the residue was extracted with ethyl acetate. The organic layer was dried over MgSO4, filtered and concentrated to yield the title compound (1.58 g, 75%> yield): ES-MS (m/z) 167 [M+H]+.
B. N-(4-Fluorophenyl)-2-(4-hydroxy-3-methylphenyl)-N-{2-[3- methoxyphenyllethyl} acetamide The title compound was prepared as described in Example 34.B using 4- hydroxy-3-methylphenylacetic acid (1.5 g, 9 mmol) to provide the_ title compound (2 g, 84% yield): ES-MS (m z) 394 [M+H]+.
C. 2-(4-Fluorophenyl)-l-(4-hydroxy-3-methylbenzyl)-6-methoxy-l, 2, 3,4- tetrahydroisoquinoline The title compound was prepared as described in Example 34. E using N-
(4-fluorophenyl)-2-(4-hydroxy-3-methylphenyl)-N-{2-[3- methoxyphenyl]ethyl} acetamide (2 g, 6 mmol) to provide the title compound (0.4 g,
18% yield): ES-MS (m/z) 378 [M+H]+.
D. 2-(4-Fluorophenyl)-6-methoxy-l-{3-methyl-4-[(2-piperidyl)ethoxy]benzyl}- 1 ,2,3,4-tetrahydroisoquinoline
The title compound was prepared as described in Example 3.D using 2- (4-fluorophenyl)- 1 -(4-hydroxy-3-methylbenzyl)-6-methoxy- 1 , 2,3 ,4-tetrahydro- isoquinoline (0.4 g, 1 mmol) to provide the title compound (0.515 g, 99% yield): ES- MS (m z) 489 [M+H]+.
EXAMPLE 41 SYNTHESIS OF 2-(4-FLUOROPHENYL)-1- {3-METHYL-4-[(2-PIPEPJDYL)ETHOXY]BENZYL}-
1 ,2,3 ,4-TETRAH YDROISOQUINOLIN-6-OL
The title compound was prepared as described in Example 2 using 2-(4- fluorophenyl)-6-methoxy-l-{3-methyl-4-[(2-piperidyl)ethoxy]benzyl}-l, 2, 3,4- tetrahydroisoquinoline (0.5 g, 1 mmol) to provide the title compound (0.14 g, 30%> yield): ES-MS (m/z) 475 [M+H]+.
EXAMPLE 42 SYNTHESIS OF 2-(2-PHENYLETHYL)-1- {4-[2-PIPERIDYL)ETΉOXY]BENZΎL}-1 ,2,3,4-
TETRAHYDROISOQUTNOLΓN-6-OL
A. 2 - [3 -(Phenylmethoxy)phenyl] ethylamine
A solution of 3-benzyloxyphenylacetonitrile (1 1.50 g, 51.50 mmol) in 100 mL of THF at 0°C was treated with LiAlFL (3.90 g, 103 mmol) in several portions over 20 minutes. The reaction mixture was warmed to room temperature and stirred for 30 minutes then it was heated at reflux for 6 h. The suspension was cooled to room temperature and quenched by the slow addition of Na2SO #10H2O (25 g). The resulting mixture was diluted with 200 mL of CH2CI2. The organic layer was separated and the remaining salt was rinsed with additional CH2CI2 (2 x 50 mL). The combined organic layers were dried over MgSO4, concentrated, and purified by column chromatography (SiO2, hexanes/ethyl acetate, 2:1) to provide the title compound (5.85 g, 51% yield): ES-MS (m/z) 228 [M+ H]+.
B. 6-Methoxy-2-(2-phenylethyl)-l-[4-(phenylmethoxy)benzyl|-l, 2,3,4- tetrahydroisoquinoline
The title compound was prepared as described in Example 14.C, using 2-
[3-(phenylmethoxy)phenyl]ethylamine (6.4 g, 1.11 mmol) to yield the title compound (0.39 g, 76% yield).
C 6-Methoxy-2-(2-phenylethyl)-2-(4-hydroxyphenyl)- 1 ,2,3 ,4- tetrahydroisoquinoline
A solution of 6-methoxy-2-(2-phenylethyl)-l-[4-
(phenylmethoxy)benzyl]- 1,2,3,4-tetrahydroisoquinoline (0.3 g, 0.67 mol) in a 1 :1 mixmre of THF and ethanol was placed under a nitrogen atmosphere. To the flask was added the palladium (10%> wt. on activated carbon, 0.100 g). The flask was evacuated,
and the mixture placed under a hydrogen atmosphere. After stirring for five hours the reaction was filtered through celite then concentrated to yield the title compound (0.05 g, 20% yield): ES-MS (m/z) 374 [M+H]+.
D. 2-(2-Phenylethyl)- 1 - {4-[(2-piρeridyl)ethoxy]benzyl} - 1 ,2,3,4- tetrahydroisoquinolin-6-ol
6-Methoxy-2-(2-phenylethyl)-l {[4-(2-piperidylethoxy)phenyl]methyl}-
1,2,3,4-tetrahydroisoquinoline was prepared as described in Example 14.E, using 6- methoxy-2-(2-phenylethyl)-2-(4-hydroxyphenyl)- 1 ,2,3,4-tetrahydroisoquinoline (0.05g,
0.13 mmol). The title compound was prepared as described in Example 14. F, using 6- methoxy-2-(2-phenylethyl)-l {[4-(2-piperidylethoxy)phenyl]methyl}-l, 2,3,4- tetrahydroisoquinoline (0.068 g, 0.14 mmol) to yield the title compound (0.015 g,
22.8% yield): Η NMR (CDC13) 6.4-7.3 (m, 12H), 4-4.2 (m, IH), 2.7-2.9 (m, 10H), 2.4-
2.7 (m, 6H), 1.5-1.7 (m, IH), 1.4-1.5 (m, 2H), 1.2 (m, 2H).
EXAMPLE 43 SYNTHESIS OF 2-(4-CHLOROPHENYL)-1-{4-[(2-PIPERIDYL)ETHOXY]BENZYL}-1,2,3,4-
TETRAHYDROISOQUINOLIN-6-OL
A. N-(4-Chlorophenyl)-2-(3-hydroxyphenyl)acetamide
The title compound was prepared as described in Example 34.B, using 4- chloroaniline (1.28 g, 10.0 mmol) to provide the title compound (2.361 g, 90% yield): ES-MS (m/z) 262 [M+H]+.
B. N-(4-Chlorophenyl)-2-[3-(phenylmethoxy)phenyl]acetamide
The title compound was prepared as described in Example 34. C, using N-(4-chlorophenyl)-2-(3-hydroxyphenyl)acetamide (2.36 g, 9.0 mmol) to provide the
title compound (2.517 g, 80% yield): Η NMR (CDC13) 7.30-7.44 (m, 7H), 7.24 (m, 3H), 7.04 (br, IH), 6.93 (m, 3H), 5.09 (s, 2H), 3.70 (s, 2H); ES-MS (m/z) 352 [M+H]+.
C. (4-Chlorophenyl){2-[3-(phenylmethoxy)phenyl]ethyl} amine
The title compound was prepared as described in Example 34.D, using N-(4-chlorophenyl)-2-[3-(phenylmethoxy)phenyl]acetamide (1.8 g, 5.1 mmol) to provide the title compound (1.251 g, 73% yield): ES-MS (m/z) 338 [M+H]+.
D. 2-(4-Chlorophenyl)-6-(phenylmethoxy)-l-{4-[(2-piperidyl)ethoxy]benzyl}- 1,2,3,4-tetrahydroisoquinoline
The title compound was prepared as described in Example 34.E, using (4-chlorophenyl){2-[3-(phenylmethoxy)phenyl]ethyl} amine (0.60 g, 1.78 mmol) to provide the title compound (0.283 g, 28% yield): lH NMR (CDC13) 7.32-7.44 (m, 5H),
7.15 (d, 2H), 6.87 (d, 2H), 6.69-6.77 (m, 7H), 5.02 (s. 2H), 4.73 (t, IH), 4.07 (t, 2H),
3.56 (m, IH), 3.45 (m, IH), 3.10 (dd, IH), 2.91 (m, 2H), 2.76 (t, 2H), 2.74 (m, IH),
2.51 (m, 4H), 1.61 (m, 4H), 1.46 (m, 2H); ES-MS (m/z) 567 [M+H]+. E. 2-(4-Chlorophenyl)- 1 - {4-[(2-piperidyl)ethoxy]benzyl} - 1 ,2,3,4- tetrahydroisoquinolin-6-ol
The title compound was prepared as described in Example 14.D, using 2- (4-chlorophenyl)-6-(phenylmethoxy)- 1 - {4-[(2-piperidyl)ethoxy]benzyl} - 1 ,2,3,4- tetrahydroisoquinoline (0.27 g, 0.47 mmol) to provide the title compound (0.98 g, 41% yield): ): Η NMR (CDCI3) 7.18 (dd, IH), 6.83 (m, 2H), 6.72 (d, 2H), 6.37-6.66 (m, 7H), 4.70 (t, IH), 4.32 (t, 2H), 3.72 (m, 3H), 3.42-3.60 (m, 2H.), 2.80-2.92 (m, 3H), 2.77-2.87 (m, 3H), 2.65 (m, IH), 1.87-2.05 (m, 6H); ES-MS (m/z) 477 [M+H]+.
EXAMPLE 44 SYNTHESIS OF 2-(3,4-DICHLOROPHENYL)- 1 - {4-[(2-PIPERIDYL)ETΉOXY]BENZYL}-1 , 2,3,4-
TETRAHYDROISOQUINOLIN-6-OL
A. N-(3,4-Dichlorophenyl)-2-(3-hydroxyphenyl)acetamide
To a solution of 3-hydroxyphenyl acetic acid (5.0 g, 0.03 mol) in DMF (50ml) was added 1-hydroxybenzotriazole hydrate (4.86 g, 0.03 mol) and l-[3- (dimethyl.amino)propyl]-3-ethylcarbodiimide hydrochloride (6.9 g, 0.036mol). To the flask was added 3, 4-di chloroaniline (4.86 g, 0.03 mol). The reaction was allowed to stir overnight. Solvent was removed and the reaction was diluted with ethyl acetate. The reaction mixture was washed with IN HC1, 10% sodium carbonate solution, and brine. The organic layer was dried over MgSO , filtered and concentrated to provide the title compound (5.5 g, 62% yield): ES-MS (m/z) 296 [M+H]+.
B. N-(3,4-Dichlorophenyl)-2-[3-(phenylmethoxy)phenyl]acetamide To a solution of N-(3,4-dichlorophenyl)-2-(3-hydroxyphenyl)acetamide
(5.5 g, 0.019 mol) in DMF (25 ml) was added potassium carbonate powder (3.93 g, 0.028 mol). To the flask was added benzyl bromide (2.37 ml, 0.021 mol). The reaction was allowed to stir overnight. Solvent was removed and the reaction was diluted with ethyl acetate. The organic layer was washed with water, dried over MgSO4, filtered and concentrated. The crude product was triturated with ether and hexanes to provide the title compound (4.65 g, 64% yield): ES-MS (m/z) 386 [M+H]+.
C. (3,4-Dichlorophenyl){2-[3-(phenylmethoxy)phenyl]ethyl} amine
To a solution of N-(3,4-dichlorophenyl)-2-[3-
(phenylmethoxy)phenyl]acetamide (4.5 g, 0.012 mol) in THF (20 ml) on ice was added the borane-tetrahydrofuran complex (15 ml, 0.023 mol). The reaction was allowed to
reflux at 80°C for six hours. The reduction reaction was placed on ice, acidified using 4 N HC1, then stirred for twenty minutes. The reaction was then basified with an aqueous solution of potassium hydroxide. The reaction was diluted with water and extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO , filtered and concentrated to provide the title compound (4.3 g, 99% yield): ES-MS (m/z) 372 [M+H]+.
D. N-(3,4-Dichlorophenyl)-2-(4-hydroxyphenyl)-N-{2-[3- (phenylmethoxy)phenyl]ethyl } acetamide
To a solution of (3,4-dichlorophenyl){2-[3- (phenylmethoxy)phenyl] ethyl} amine (4.32 g, 0.011 mol) in chlorobenzene (40 ml) was added 4-hydroxy phenyl acetic acid (2.43 g, 0.014 mol), followed by phosphorus trichloride (5 ml, 0.005 mol). The reaction was allowed to reflux at 135 °C overnight.
Solvent was removed and the reaction was basified with 10 % sodium hydroxide solution. The reaction was diluted with ethyl acetate and water. The organic was washed with brine, dried with MgSO4, filtered, and concentrated to provide the title compound (5.5 g, 99% yield): ES-MS (m/z) 506 [M+Hf.
E. 2-(3,4-Dichlorophenyl)-l-(4-hydroxybenzyl)-6-(phenylmethoxy)-l, 2, 3,4- tetrahydroisoquinoline
To a solution of N-(3,4-dichlorophenyl)-2-(4-hydroxyphenyl)-N-{2-[3- (phenylmethoxy)phenyl]ethyl}acetamide (7.6 g,.015 mol) in acetonitrile (30 ml) was added phosphorus oxychloride (4.19 ml, 0.045 mol). The reaction was allowed to reflux at 80°C for 6 hours. Solvent was removed and the reaction was placed on ice. To the flask was added ice and water. The reaction was extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO , filtered, concentrated, and then dissolved in methanol. To the flask was added small aliquots of sodium borohydride (1.02 g, 0.027 mol). The reaction was allowed to stir overnight. The solvent was removed and the reaction was diluted with dichloromethane and water. The organic layer was separated and the aqueous layer was extracted with additional dichloromethane. The organic layers were combined, washed with brine, dried over MgSO4, filtered and concentrated to provide the title compound (0.5 g, 6.8%o yield): ES- MS (m/z) 490 [M+H]+.
F. 2-(3,4-Dichlorophenyl)-6-(phenylmethoxy)-l-{4-[2-piperidyl)ethoxy1benzyl}- 1 ,2, 3,4-tetrahydroisoquinoline
To a solution of 2-(3,4-dichlorophenyl)-l-(4-hydroxybenzyl)-6-
(phenylmethoxy)- 1,2,3,4-tetrahydroisoquinoline (0.5 g, 0.001 mol) in DMF (3ml) was added potassium carbonate (0.2 g, 0.0015 mol). The reaction was allowed to stir for twenty minutes. To the flask was added l-(2-chloroethyl)piperidine monohyrdochloride (0.22 g, 0.0012 mol) The reaction was allowed to stir at 80°C overnight. Solvent was removed. The reaction was diluted with ethyl acetate and water. The aqueous layer was extracted with ethyl acetate. The organic layers were combined, washed with brine, dried over MgSO , filtered and concentrated to yield the title compound (0.42 g, 70% yield): ES-MS (m/z) 601 [M+H]+.
G. 2-(3,4-Dichlorophenyl)-l-{4-[(2-piperidyl)ethoxylbenzyl}-l,2,3,4- tetrahydroisoquinolin-6-ol
A solution of 2-(3,4-dichlorophenyl)-6-(phenylmethoxy)-l-{4-[(2- piperidyl)ethoxy]benzyl}-l,2,3,4-tetr,ahydroisoquinoline (0.380 g, 0.63 mmol) was placed under a nitrogen atmosphere and dissolved in ethyl acetate (5 ml). The flask was evacuated and flushed with nitrogen. To the flask was added palladium (10% wt. on activated carbon, 0.190 g). The flask was flushed and evacuated with nitrogen followed by hydrogen. The reaction was allowed to stir under the hydrogen atmosphere at room temperature for 5 hours. The reaction mixmre was filtered through celite and concentrated. The product was purified by preparative HLPC (C-18 column, 10-100%) acetonitrile/water with 0.1% trifluoroacetic acid) to provide the title compound (0.010 g, 3% yield). 1H NMR (CDC13) 6.7-7.2 (m, 10H), 4.7 (t, IH), 4.2-4.4 (m, 2H), 3.6-4.0
(m, 4H), 3.3-3.6 (m, 3H), 3.0-3.1 (m, IH), 2.7-2.9 (m, 3H), 2.6-2.7 (m, IH), 1.8-2.1 (m, 4H), 1.4 (m, 2H); ES-MS (m/z) 511 [M+H]+.
EXAMPLE 45 SYNTHESIS OF 2-(4-FLUOROPHENYL)-1- {4-[(2-PIPERIDYL)ETHOXY]PHENETHYL}-1 ,2,3,4-
TETRAHYDROISOQUINOLIN-6-OL
A. N-(4-Fluorophenyl)-3-(4-hydroxyphenyl)-N-{2-[3- (phenylmethoxy)phenyl]ethyl}propanamide
The title compound was prepared as described in Example 44.D using
(4-fluorophenyl){2-[3-(phenylmethoxy)phenyl]ethyl} amine (1.4 g, 4.36 mmol) and 3-
(4-hydroxyphenyl)propanoic acid (1.01 g, 6.11 mmol) to provide the title compound (1.82 g, 89% yield): ES-MS (m/z) 470 [M+H]+.
B. 2-(4-Fluorophenyl)- 1 -(4-hydroxyphenethyl } -6-phenylmethoxy- 1 ,2, 3,4- tetrahydroisoquinoline
The title compound was prepared as described in Example 14.B using N- (4-fluoropheny l)-3-(4-hydroxyphenyl)-N- {2 - [3 -(phenylmethoxy)phenyl] ethyl } - propanamide (1.81 g, 3.85 mmol) to provide the title compound (0.78 g, 45% yield): ES-MS (m/z) 454 [M+H]+.
C. 2-(4-Fluorophenyl)-6-phenylmethoxy-l-{4-[(2-piperidyl)ethoxy]phenethyl}- 1 ,2,3,4-tetrahydroisoquinoline
The title compound was prepared as described in Example 3.D using 2- (4-fluorophenyl)- 1 -(4-hydroxyphenethyl)-6-phenylmethoxy- 1 ,2,3,4-tetrahydroisoquinoline (0.76 g, 1.67 mmol) to provide the title compound (0.50 g, 53%o yield: ES- MS (m/z) 565 [M+H]+.
D. 2-(4-Fluorophenyl)- 1 - {4-[(2-piperidyl)ethoxy]phenethyl} - 1 ,2,3,4- tetrahydroisoquinolin-6-ol
The title compound was prepared as described in Example 14.D using 2-
(4-fluorophenyl)-6-phenylmethoxy- 1 - {4-[(2-piperidyl)ethoxy]phenethyl } - 1 ,2,3 ,4- tetrahydroisoquinoline (0.50 g, 0.89 mmol) to provide the title compound (0.172 g, 41%> yield: ES-MS (m z) 475 [M+H]+.
EXAMPLE 46
SYNTHESIS OF 2-(4-FLUOROPHENYL)-1 - {4-(N-ACETYL)BENZYL} -1 ,2,3,4-
TETRAHYDROISOQUINOLIN-6-OL
A. 2-(4-Fluorophenyl)-6-phenylmethoxy-l - {4-aminobenzyl}-l ,2,3,4- tetrahydroisoquinoline
A solution of 2-(4-fluorophenyl)-6-phenylmethoxy-l-{4-nitrobenzyl}-
1,2, 3,4-tetrahydroisoquinoline (3g, 6.4 mmol) and SnC^'^O (7.2 g, 32 mmol) in DMF was stirred at room temperature overnight. The solvent was removed and the residue was treated with ethyl acetate (200ml) and water (200 ml). The organic layer was dried over MgSO , filtered and concentrated to provide the title compound (2.8 g, 100% yield): ES-MS (m/z) 439 [M+H]+.
B. 2-(4-Fluorophenyl)-6-phenylmethoxy-l-[4-(N-acetyl)benzyl]-l,2,3,4-tetrahydro isoquinoline
A solution of 2-(4-fluorophenyl)-6-phenylmethoxy-l-{4-aminobenzyl}-
1,2, 3,4-tetrahydroisoquinoline (0.56 g, 1.3 mmol), AC2O (3 ml) and pyridine (2.6 ml) were stirred at room temperature for 3 hours. The solvents were removed and the residue treated with water and ethyl acetate. The organic layer was dried over MgSO , filtered, concentrated and purified by column chromatography (SiO2, ethyl acetatε
:hexanes, 2:3) to provide the title compound (0.39 g, 62% yield): ES-MS (m/z) 481 [M+H]+.
C. 2-(4-Fluorophenyl)-l-{4-(N-acetyl)benzyl}-l,2,3,4-tetrahydroisoquinolin-6-ol
The title compound was prepared as described in Example 14.D using 2- (4-fluorophenyl)-6-phenylmethoxy- 1 - {4-(N-acetyl)benzyl } - 1 ,2,3 ,4- tetrahydroisoquinoline (0.39 g., 0.8 mmol) to provide the title compound (0.28 g, 88% yield): ES-MS (m/z) 390 [M+H]+.
EXAMPLE 47 SYNTHESIS OF 2-(4-FLUOROPHENYL)- 1-(4-[2-(1-METHYL(2- PIPERID YL))ETHOX Y]BENZ YL)- 1 ,2,3 ,4-TETRAHYDROISOQUINOLIN-6-OL
A. N-(4-Fluorophenyl)-2-(3-hydroxyphenyl)acetamide
The title compound was prepared as described in Example 44. A, using 3- hydroxyphenyl acetic acid (80 g, 0.52 mol) and 4-fluoroaniline (49.3 ml, 0.52 mol) to provide the title compound (113 g, 89% yield): ES-MS (m/z) 246 [M+H]+.
B. N-(4-Fluorophenyl)-2-[3-(phenylmethoxy)phenyl]acetamide
The title compound was prepared as described in Example 44.B, using N-(4-fluorophenyl)-2-(3-hydroxyphenyl)acetamide (335 g, 1.36 mol) to provide the title compound (345 g, 75% yield): ES-MS (m/z) 336 [M+H]+. C. (4-Fluorophenyl) {2-[3-(phenylmethoxy)phenyl]ethyl} amine
The title compound was prepared as described in Example 44. C, using N-(4-fluorophenyl)-2-[3-(phenylmethoxy)phenyl]acetamide (73.65 g, 0.22 mol) to provide the title compound (70.38 g, 99% yield): ES-MS (m/z) 322 [M+H]+.
D. N-(4-Fluorophenyl)-2-(4-hydroxyphenyl)-N-{2-[3- (phenylmethoxy)phenyl]ethyl} acetamide
The title compound was prepared as described in Example 44.D, using (4-fluorophenyl){2-[3-(phenylmethoxy)phenyl]ethyl} amine (62 g, 0.19 mol) to provide the title compound (86 g, 99% yield): ES-MS (m/z) 456 [M+H]+.
E. 2-(4-Fluorophenyl)-l-(4-hydroxybenzyl)-6-(phenylmethoxy)- 1,2,3,4- tetrahydroisoquinoline
The title compound was prepared as described in Example 44. E, using
N-(4-fluorophenyl)-2-(4-hydroxyphenyl)-N-{2-[3- (phenylmethoxy)phenyl]ethyl} acetamide (86.45 g, 0.19 mol) to yield the title compound (22 g, 26% yield): ES-MS (m/z) 440 [M+H]+.
F. 2-(4-Fluorophenyl)-l-(4-[2-(l-methyl(2-piperidyl))ethoxy]benzyl)-6- (phenylmethoxy)-l, 2, 3,4-tetrahydroisoquinoline
To a solution of 2-(4-fluorophenyl)-l-(4-hydroxybenzyl)-6- (phenylmethoxy)- 1,2, 3,4-tetrahydroisoquinoline (0.500 g, 1.14 mmol) in DMF (5 ml) was added potassium carbonate (0.236 g, 1.7 mmol) and the resulting mixture allowed to stir for twenty minutes. To the reaction mixture was added 2-(2-chloroethyl)-N- methyl piperidine (0.271 g, 1.37 mmol). The reaction was allowed to stir overnight. The reaction was diluted with water and extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO , filtered, and concentrated. The product was purified by radial chromatography (100% CH2C12, then CH2Cl2/MeOH, 95:5) to yield the title compound (0.043 g, 7% yield): ES-MS (m/z) 565 [M+H]
G. 2-(4-Fluorophenyl)- 1 -(4-[2-( 1 -methyl(2-piperidyl))ethoxy]benzyl)- 1 ,2,3 ,4- tetrahydroisoquinolin-6-ol The title compound was prepared as described in Example 44. G, using 2-
(4-fluorophenyl)- 1 -(4-[2-( 1 -methyl(2-piperidyl))ethoxy]benzyl)-6-(phenylmethoxy)-
1,2,3,4-tetrahydroisoquinoline (0.043 g, 0.076 mmol). The product was purified by radial chromatography (100% CH2C12, then CH:Cl2/MeOH, 95:5) to yield the titlε compound (0.005 g, 14 % yield): ES-MS (m/z) 475 [M+H]+.
EXAMPLE 48 SYNTHESIS OF 2-(4-FLUOROPHENYL)-1- {2-[(2-PIPERIDYL)ETHOXY]BENZYL} -1,2,3,4-
TETRAHYDROISOQUTNOLIN-6-OL
A. N- {2-(3-Methoxyphenyl)ethyl } -N-(4-fluorophenyl)-2- {2- (phenylmethoxy)phenyl } acetamide
The title compound was prepared as described in Example 3. A using 2- benzyloxyphenylacetyl chloride (2.44 g, 10 mmol) to yield the title compound (4.44 g, 94% yield): ES-MS (m/z) 470[M+Hf. B. l-[2-(Phenylmethoxy)benzyl]-6-methoxy-2-fluorophenyl-l, 2, 3,4- tetrahydroisoquinoline
The title compound was prepared as described in Example 1.D using N- [2-(3-methoxyphenyl)ethyl]-N-(4-fluorophenyl)-2-{2-
(phenylmethoxy)phenyl} acetamide (4.4 g, 9.4 mmol) to provide the title compound (1.8 g, 42% yield): ES-MS (m/z) 454 [M+H]+.
C. 6-Methoxy-2-fluorophenyl-l-(2-hydroxybenzyl)- 1,2, 3,4-tetrahydroisoquinoline
The title compound was prepared as described in Example 3.C using 1- [2-(phenylmethoxy)benzyl]-6-methoxy-2-fluorophenyl-l, 2, 3,4-tetrahydroisoquinoline (1.8g, 4 mmol) to yield the title compound (1.37 g, 95% yield): ES-MS (m/z) 364
D. 6-Methoxy-2-fluorophenyl- 1 - {2-[(2-piperidyl)ethoxy]benzyl } - 1 ,2, 3,4- tetrahydroisoquinoline
The title compound was prepared as described in Example 3.D using 6- mεthoxy-2-fluorophεnyl-l-(2-hydroxybenzyl)-l,2,3,4-tetrahydroisoquinoline (1.37g, 3.7 mmol) to provide the title compound (1.7g, 95% yield): ES-MS (m/z) 475 [M+H]+.
E. 2-(4-Fluorophenyl)- 1 - {2-[(2-piperidyl)ethoxy]benzyl } - 1 ,2,3,4- tetrahydroisoquinolin-6-ol
The title compound was prepared as described in Example 2 using 6- methoxy-2-fluorophεnyl-l- {2-[(2-piperidyl)ethoxy]benzyl}-l, 2,3,4- tetrahydroisoquinoline (1 Ng, 3.5 mmol) to provide the title compound (0.112 g, 7% yield): ES-MS (m/z) 460[M+H]+.
EXAMPLE 49 SYNTHESIS OF 2-(4-FLUOROPHEΝYL)-1 - {4-(2-PIPERJDYLACETAMIDE)BEΝZYL} -1,2,3,4-
TETRAHYDROISOQUINOLIN-6-OL
A. 2-(4-Fluorophenyl)-6-phenylmethoxy-l - {4-(2-Bromoacetamide)benzyl}- 1,2.3,4-tetrahydroisoquinoline
A solution of 2-(4-fluorophenyl)-6-phεnylmethoxy-l-{4-aminobenzyl}- 1,2,3,4-tetrahydroisoquinoline (0.65g, 1.5 mmol), bromoacetylbromide (0.33g, 1.65mmol) and trielthylamine (0.17 g, 1.65 mmol) in anh THF was stirred at room temperature overnight. Excess reagent was quenched by addition of water, and the reaction extracted with CH2CI2. The organic layer was dried over MgSO and concentrated to yield the title compound (0.83 g, 99% yield): ES-MS (m/z) 559/561 [M+H]+. B. 2-(4-Fluorophenyl)-6-phenylmεthoxy-l-[4-(2-piperidylacetamide)benzyl]- 1 ,2,3 ,4-tetrahydroisoquinoline
A mixture of 2-(4-fluorophenyl)-6-phenylmethoxy-l-[4-(2- bromoacetamide)benzyl]- 1,2, 3,4-tetrahydroisoquinoline (0.83 g, 1.5 mmol ), piperidinε
(0.133g, 1.6 mmol) and K2CO3 (0.25 g, 1.8 mmol) in CH2G2 was stirred at room temperature overnight. The reaction mixture was concentrated and purified by column
chromatography (SiO2, CH2Cl2/MeOH, 12: 1) to provide the title compound (0.2 g. 24% yield): ES-MS (m/z) 564 [M+H]+.
C. 2-(4-Fluorophenyl)-l-{4-(2-piperidylacetamide)benzyl}-l,2,3,4-tetrahydroiso quinolin-6-ol The title compound was prepared as described in Example 3.D using 2-
(4-fluorophenyl)-6-phenylmethoxy- 1 - {4-(2-piperidylacetamide)benzyl} - 1 ,2,3 ,4- tetrahydroisoquinoline (0.05 g, 0.09 mmol) to provide the title compound (0.04 g, 95% yield): ES-MS (m/z) 474 [M+H]+.
EXAMPLE 50 SYNTHESIS OF 2-(4-FLUOROPHENYL)- 1 -[4-(1 -METHYLPYRROLIDIN-3-YLOXY)BENZYL]-
1 ,2,3,4-TETRAHYDROQUINOLIN-6-OL
A. 2-(4-Fluorophenyl)-l-[4-(l-methylpyrrolidin-3-yloxy)benzyl]-6- (phenylmethoxy)- 1,2,3,4-tetrahydroisoquinoline To a solution of 2-(4-fluoroρhenyl)-l -(4-hydroxybenzyl)-6-
(phenylmethoxy)- 1,2, 3,4-tetrahydroisoquinoline (0.450 g, 1.02 mmol) in THF (5 ml) was added l-methyl-3-pyrrolidinol (0.22 ml, 2.04 mmol), tri-n-butyl-phosphine (0.5ml, 2.04 mmol) and 1,1 ' azodicarbonyl dipiperidine (0.5 g, 2.04 mmol) respectively. Dichloromethane (4 ml) was added and the reaction was allowed to stir overnight. The reaction was diluted with aqueous sodium bicarbonate and extracted with ethyl acetate. The organic layer was dried v/ith MgSO , filtered and concentrated. The product was purified by radial chromatography (100% CH2C1 , then CH2Cl2/MeOH, 95:5) to yield the title compound (0.30 g, 56% yield): ES-MS (m/z) 523 [M+Hf.
B. 2-(4-Fluorophenyl)-l-[4-(l-methylpyrrolidin-3-yloxy)benzyl]-l, 2,3,4- tetrahydroisoquinolin-6-ol
The title compound was prepared as described in Example 44. G, using 2-
(4- fluorophenyl)- 1 -[4-( 1 -methylpyrrolidin-3-yloxy)benzyl]-6-(phenylmethoxy)- 1 ,2,3,4- tetrahydroisoquinoline (0.265 g, 0.5 mmol) to provide the title compound (0.005 g, 2% yield): Η NMR (CDC13) 6.7-7.2 (m, 11H), 5.1 (m, IH), 4.9 (m, IH), 3.7 (m, 2H), 3.0
(m, 6H), 2.4 (m, 2H), 1.4-1.7 (m, 5H); ES-MS (m/z) 433 [M+H]+.
EXAMPLE 51 SYNTHESIS OF 2-(4-FLUOROPHENYL)-1-[4-(2-PIPERIDYLETHOXY)BENZYL]-6-1 ,2,3,4- TETRAHYDROISOQUINOLYL MELTHYLSULFONATE
A. 2-(4-Fluorophenyl)-6-(phenylmethoxy)-l-{4-[(2-piperidyl)ethoxy]benzyl}- 1 ,2, 3,4-tetrahydroisoquinoline
The title compound was prepared using the procedure described in Example 44.F, using 2-(4-fluorophenyl)-l-(4-hydroxybenzyl)-6-(phenylmethoxy)- 1,2, 3,4-tetrahydroisoquinoline (15.6 g, 0.036 mol) to provide the -title compound (8.5 g, 43% yield): ES-MS (m/z) 551 [M+H]+.
B. 2 -(4-Fluorophenyl)- 1 - {4-[(2-ρiρeridyl)ethoxy]benzyl} - 1 ,2,3,4- tetrahydroisoquinolin-6-ol The title compound was prepared using the procedure described in
Example 44. G, using 2-(4-fluorophenyl)-6-(phenylmethoxy)-l-{4-[(2- piperidyl)ethoxy]benzyl}- 1,2,3,4-tetrahydroisoquinoline (8.4 g, 0.018 mol) to provide the title compound (6.0 g, 87% yield): ES-MS (m/z) 461 [M+H]+.
C. 2-(4-Fluorophenyl)-l-[4-(2-piperidylethoxy)benzyl]-6-l,2,3,4- tetrahydroisoquinolyl methylsulfonatε
To a solution containing 2-(4-fluorophenyl)-l-{4-[(2- piperidyl)ethoxy]benzyl}-l,2,3,4-tetrahydroisoquinolin-6-ol (0.100 g, 0.2 mmol) in pyridine (0.4 ml) was added methyl sulfonyl chloride (25 μl, 0.32mmol). After stirring for five hours, solvent was removed and the reaction was basified with aqueous sodium bicarbonate solution. The reaction was extracted with dichloromethane and concentrated. The product was purified by semipreparative HLPC (C-18 column, 10- 100% acetonitrile/water with 0.1% trifluoroacetic acid). The acetonitrile was removed from the HPLC fractions containing the desired product. Ethyl acetate was added and the solution neutralized using saturated sodium bicarbonate. The organic layer was washed with brine, dried over MgSO , filtered and concentrated to provide the title compound (0.0135 g, 13% yield): 1H NMR (CDC13) 6.7-7.1 (m, 11H), 4.78 (t,lH), 4.1 (t, 3H), 3.45-3.62 (m, 2H), 2.62-3.18 (m, 8H), 2.58 (m, 4H), 1.63 (m, 4H), 1.43 (m, 2H); ES-MS (m z) 539 [M+H]+.
EXAMPLE 52 SYNTHESIS OF 2-(2,4-DICHLOROPHENYL)- 1 - {4-[(2-PIPERIDYL)ETHOXY]BENZYL} - 1 ,2,3,4-
TETRAHYDROISOQUINOLIN-6-OL
A. Phenylmethyl 2- 3-(phenylmethoxy)phenyl]acetate
To a solution of 3-hydroxyphenyl acetic acid (5.0 g, 0.03 mol) in DMF (25 ml) was added potassium carbonate (12.4 g, 0.09 mol). The reaction was allowed to stir for twenty minutes at which time benzyl bromide (8.9 ml, 0.075 mol) was added to the flask. The reaction was allowed to stir overnight. Solvent was removεd. The rεaction was diluted with water and extracted with ethyl acetate. The organic layer was
washed with brine, dried over MgSO , filtered and concentrated to yield the title compound (9.9 g, 99% yield): ES-MS (m/z) 243 [M+Hf.
B. 2-[3-(Phenylmethoxy)phenyl]acetyl chloride
To a solution of phenylmethyl 2-[3-(phenylmethoxy)phenyl]acetate (9.97 g, 0.03 mol) in a 5:1 mixmre of THF/water was added a solution of lithium hydroxide monohydrate (2.5 g, 0.06 mol) in water. The reaction was allowed to stir at 50 °C for 6 hours and then at room temperature overnight. Solvent was removed and the reaction was acidified with 4 N HC1 solution while on ice. 2-[3- (Phenylmethoxy)phenyl]acetic acid precipitated from the solution and was collected by filtration. The 2-[3-(phenylmethoxy)phenyl]acetic acid (7.0 g, 0.03 mol) was dissolved in dichloromethane (100 ml) and a small amount of DMF (4 drops) was added. To the reaction was added oxalyl chloride (5.23 ml, 0.06 mol). The reaction was allowed to stir for 6 hours, and solvents were removed to yield the title compound (7.7 g, 99%> yield): ES-MS (m/z) 386 [M+H]+. C. N-(2,4-Dichloropher.yl)-2-[3-(phenyImethoxy)phenyl}acetamide
To a solution of 2,4-dichloroaniline (2.67 g, 0.0165 mol) in dichloromethane (20 ml) was slowly added a solution of 2-[3- (phenylmethoxy)phenyl]acetyl chloride (3.84 g, 0.015 mol) in dichloromethane (10 ml). After stirring for three hours, triethylaminε (2 ml, 0.015 mol) was added to the reaction and the reaction was allowed to stir overnight. To the reaction was added an aqueous solution of sodium bicarbonate. The mixture was extracted with dichloromethane. The organic layer was washed with brine, dried over MgSO4, filtered and concentrated. The solid was triturated with ether and hexane, then filtered to provide the title compound (4.0 g, 70% yield): ES-MS (m/z) 372 [M+H]+. D. (2,4-Dichlorophenyl)-2-(4-hydroxyphenyl)-N-2{2-[3- (phenylmethoxy)phenyl]ethyl} acetamide
The title compound was prepared as described in Example 44.D, using
N-(2,4-dichlorophenyl)-2-[3-(phenylmethoxy)phenyl} acetamide (4.0 g, 0.01 mol) to provide the title compound (3.72 g, 44% yield): ES-MS (m/z) 506 [M+H]+.
E. 2-(2,4-Dichlorophenyl)-l-(4-hydroxybenzyl)-6-(phenylmethoxy)- 1,2,3,4- tetrahydroisoquinoline
The title compound was prepared as described in Example 44. E, using
(2,4-dichloroρhenyl)-2-(4-hydroxyphenyl)-N-2{2-[3- (phenylmethoxy)phenyl]ethyl} acetamide (3.5 g, 0.009 mol) to provide the title compound (1.0 g, 22% yield): ES-MS (m/z) 490 [M+H]+.
F. 2-(2,4-Dichlorophenyl)-6(phenylmethoxy)-l-{4-[(2-piperidyl)ethoxy}benzyl}- 1 ,2,3,4-tetrahydroisoquinoline
The title compound was prepared as described in Example 44.F, using 2- (2,4-dichlorophenyl)- 1 -(4-hydroxybenzyl)-6-(phenylmethoxy)- 1 ,2,3 ,4- tetrahydroisoquinoline (0.96 g, 0.002 mol) to providε thε title compound (1.2 g, 50 % yield): ES-MS (m/z) 601 [M+H]+.
G. 2-(2 ,4-Dichlorophenyl)- 1 - {4- [2-piperidyl)ethoxy]benzyl } - 1 ,2,3 ,4- tetrahydroisoquinolin-6-ol The title compound was prepared as described in Example 44. G, using 2-
(2,4-dichlorophenyl)-6-(phenylmethoxy)- 1 - {4-[(2-piperidyl)εthoxy } benzyl} - 1 ,2,3,4- tetrahydroisoquinoline (0.60 g, 1 mmol) to provide the title compound (0.0083 g, 1.6 % yield): IH NMR (CDC13) 6.7-7.0 (m, 10H), 4.2 (t, IH). 4.1 (t, 2H), 3.4-3.7 (m, 2H), 3.05 (m, 2H), 2.4-2.9 (m, 8H), 1.7 (m, 4H), 1.5 (m, 2H); ES-MS (m/z) 511 [M+H]+.
EXAMPLE 53
SYNTHESIS OF 2-(4-FLUOROPHENYL)-1- {[4-(2-PIPERIDYL)ETHOXY]BENZYL} -6-1 ,2,3,4- TETRAHYDROISOQUINOLYL AMINOSULFONATE
To a solution of chlorosulfonyl isocyanate (100 μl, 1.08 mmol) in toluene (2ml) cooled in a dry ice/acetone bath was added formic acid (40 μl, 1.08 mmol). The reaction was allowed to stir at room temperature for three hours. The
reaction yielded N-(chlorosulfonyl)carbamoyl formate in a tolulene solution. To a solution of 2-(4-fluorophenyl)-l- {4-[(2-piperidyl)ethoxy]benzyl}- 1,2,3,4- tetrahydroisoquinolin-6-ol (0.100 g, 0.2 mmol) in pyridine was added the N- (chlorosulfonyl)carbamoyl formate solution in toluene (1.5ml). The reaction was allowed to stir for three hours. The reaction was treated with an aqueous sodium bicarbonate solution and extracted with dichloromethane. The product was purified by HPLC (C-18 column, 10-100% acetonitrile/water with 0.1%. trifluoroacetic acid) to yield the title compound (0.0083 g, 8% yield): IH NMR (CDC13) 6.6-7.2 (m, 1 IH), 2.7- 3.8 (m, 12H), 5.4 (broad s, 2H), 4.85 (t, IH), 4.3 (m, 2H), 3.4-3.8 (m, 4H), 3.1 (m, IH), 2.7-3.0 (m, 7H), 1.9 (m, 4H), 1.5 (m, 2H); ES-MS (m/z) 540 [M+H]+.
EXAMPLE 54
SYNTHESIS OF 2-(2-(4-FLUOROPHENYL)-1 - {4-[(2-PIPERIDYL)ETHOXY]BENZYL} -6-
1 ,2,3,4-TETRAHYDROISOQUTNΌLYLOXY)ACETAMIDE
To a solution of 2-(4-fluorophenyl)-l-{4-[(2-piperidyl)ethoxy]benzyl}- l,2,3,4-tetrahydroisoquinolin-6-ol (0.100 g, 0.2 mmol) in THF (1 ml) and DMF (5 drops) on ice was added sodium hydride (0.024 g, 0.6 mmol). To the flask was added bromoacetamide (0.083 g, 0.6 mmol). While warming to room temperature the reaction was allowed to stir for 6 hours. The reaction was quenched with an aqueous solution of sodium bicarbonate and extracted with dichloromethane. The organic layer was dried over MgSO , filtered and concentrated. The product was purified by HPLC as described above to yield the title compound (0.005 g, 4.8% yield): ES-MS (m/z) 518 [M+H]+.
EXAMPLE 55
SYNTHESIS OF N-(CARBAMOYLMETHYL)-2-(2-(4-FLUOROPHEN YL)- 1 - {4-[(2- PIPERIDYL)ETHOXY]BENZYL} (6-1 ,2,3,4-TETRAHYDROISOQUINOLYLOXY))ACETAMIDE
To a solution of 2-(4-fluorophenyl)-l-{4-[(2-piperidyl)ethoxy]benzyl}- l,2,3,4-tetrahydroisoquinolin-6-ol (0.100 g, 0.2 mmol) in THF (1ml) and DMF (5 drops) on ice was added sodium hydride (0.024 g, 0.6 mmol). To the flask was added bromoacetamide (0.083 g, 0.6 mmol). While warming to room temperature the reaction was allowed to sit for 6 hours. The reaction was quenched with an aqueous solution of sodium bicarbonate and extracted with dichloromethane. The organic layer was dried over MgSO , filtered and concentrated. The product was purified by semipreparative HPLC (C-18 column, 10-100% acetonitrile/water with 0.1% trifluoroacetic acid) to yield the title compound (0.008 g, 7.0% yield): IH NMR (CDC13) 6.6-7.3 (m, 11H), 6.0 (broad s, 2H), 5.55 (broad s, IH), 4.7 (t, IH), 4.5 (s, 2H), 4.1 (m, 4H), 3.5 (m, 2H), 3.05 (m, IH), 2.9 (m, 4H), 2.65 (m, IH), 2.55 (m, 4H), 1.65 (m, 4H), 1.5 (m, 2H); ES-MS (m/z) 575 [M+H]+.
11
EXAMPLE 56 SYNTHESIS OF 2-CYCLOPROPANECARBONYL- 1 - {4-[(2-PIPERIDYL)ETHOXY]BENZYL} L,2,3,4-TETRAHYDROISOQUINOLIN-6-OL
A. 2-(4-Hydroxyphenyl)-N-{2-[3-(phenylmethoxy)phenyl]ethyl} acetamide
A solution of 2-[3-(phenylmethoxy)phenyl]ethylamine (2.80 g, 12.3 mmol), 4-hydroxyphenylacetic acid (2.25 g, 14.8 mmol), N, N-diisopropylethylamine (2.79 mL, 16 mmol), and EDCI (3.07 g, 16 mmol) in 20 mL of DMF was stirred at room temperature for 10 h. The reaction mixture was poured into 100 mL of water and the aqueous layer was extracted with CH2C1?. The organic layer was dried over MgSO , concentrated, and purified by column chromatography (Siθ2, hexanes/ethyl acetate, 1 :1) to provide the title compound (2.50 g, 56% yield): ES-MS, (m/z) 362 [M+H]+.
B. l-(4-Hydroxybenzyl)-(6-phenylmethoxy)- 1,2, 3,4-tetrahydroisoquinoline The title compound was prepared as described in Example 44.E, using 2-
(4-hydroxyphenyl)-N-{2-[3-(phenylmethoxy)phenyl]ethyl}acetamide (3.69 g, 0.01 mol) to provide the title compound (0.57 g, 17% yield): ES-MS (m/z) 346 [M+H]+.
C. 2-Cyclopropanecarbonyl-l-(4-hydroxybenzyl)-(6-phenylmethoxy)- 1,2,3,4- tetrahydroisoquinoline To a solution of cyclopropane carboxylic acid (56 μl, 0.7 mmol) in DMF
(0.5 ml) was added l-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.0997 g, 0.52 mmol) followed by a solution of l-(4-hydroxybenzyl)-(6- phenylmethoxy)- 1,2, 3,4-tetrahydroisoquinoline (0.150 g, 0.43 mmol) in DMF (0.5ml). The reaction was allowed to stir overnight. Solvent was removed. The reaction was diluted with ethyl acetate, washed with 1 N HCl, 10% sodium carbonate solution, and
brine. The organic layer was dried over MgSO4, filtered and concentrated to yield the title compound (0.15 g, 84% yield): ES-MS (m/z) 414 [M+H]+.
D. 2-Cyclopropanecarbonyl-l-{[4-(2-piperidylethoxy)phenyl]methyl})-(6- phenylmethoxy)-! .2.3,4-tetrahydroisoquinoline The title compound was prepared as described in Example 44.F, using 2- cyclopropanecarbonyl-l-(4-hydroxybenzyl)-6-phenylmethoxy- 1,2,3,4- tetrahydroisoquinoline (0.15 g, 0.36 mmol) to provide the title compound (0.050 g, 27% yield): ES-MS (m/z) 525 [M+H]+.
E. 2-Cyclopropanecarbonyl- 1 - >, 4-[(2-piperidyl)ethoxy]beπz/ ' ; 1-1.2.3.4— tetrahydroisoquinolin-6-oI
The title compound was prepared as described in Example 44. G, using 2- cyclopropanecarbonyl- 1 - { [4-(2-piperidylethoxy)phenyl]methyl} )-(6-phenylmεthoxy)- 1,2,3,4-tetrahydroisoquinoline (0.050 g, 0.1 mmol) to afford the title compound (0.01 g, 22% yield): IH NMR (CDC13) 6.5-7.0 (m, 7H), 5.5 (m, 0.5 H) 5.2 (m, 0.5 H) (amide bond rotamer), 4.5-4.6 (m, IH), 4.0-4.2 (m, 2H), 3.8-3.9 (m, 0.5H), 3.6-3.7 (m, 0.5H)(amide bond rotamer), 3.0-3.2 (in, 2H), 2.5-2.9 (m, 8H), 1.6-1.8 (m, 4H), 1.1-1.4 (m, 2H), 0.6-1.1 (m, 4H), 0.5-0.6 (m, 0.5H), 0.3-0.4 (m, 0.5H) (amide bond rotamer); ES-MS (m/z) 435 [M+H]+.
EXAMPLE 57
SYNTHESIS OF 2-(2-METH YLPROPANOYL)- 1 - {4-[(2-PIPERID YL)ETHOXY]BENZYL } - 1 ,2,3 ,4-
TETRAHYDROISOQUTNOLIN-6-OL
A. 2-(2-Methylpropanoyl)- 1 -(4-hydroxybenzyl)-(6-phenylmethoxy)- 1 ,2,3,4- tεtrahydroisoquinolinε
The titlε compound was prepared as described in Example 56. C, using isobutyric acid (103 μl, 1.12 mmol) and diisopropylethyl amine (10 μl, 0.4 mol) to provide the title compound (0.054 g, 36% yield): ES-MS (m/z) 416 [M+H]+. B. 2-(2-Methylpropanoyl)-l-{4-[(2-piperidyl)ethoxy]benzyl}-l,2,3,4- tetrahydroisoquinolin-6-ol
The title compound was prepared as described in Examples 44. F and 44. G starting with 2-methylpropanoyl-l-(4-hydroxybenzyl)-(6-phenylmethoxy)- 1,2,3,4- tetrahydroisoquinoline (0.054 g, 0.13 mmol) to provide the title compound: (0.004 g, 7% yield): ES-MS (m/z) 437 [M+H]+.
EXAMPLE 58
SYNTHESIS OF 2-CYCLOHEXANECARBONYL-1 - {[4-(2-
PIPERIDYLETHOXY)PHENYL]METHYL}-1 ,2,3,4-TETRAHYDROISOQUINOLIN-6-OL
A. 2-Cyclohexanecarbonyl-l-(4-hydroxybenzyl)-6-phenylmethoxy-l,2,3,4- tεtrahydroisoquinolinε
The title compound was prepared as described in Example 56. C, using cyclohexane carboxylic acid (0.143 g, 1.12 mmol). The crude product was purified via radial chromatography to provide the title compound (0.056 g, 33% yield): ES-MS (m/z) 456 [M+H]+.
B. 2-Cyclohexanecarbonyl- 1 - { [4-(2-piperidylethoxy)phenyl]methyl } )-6- phenylmethoxy-1, 2, 3,4-tetrahydroisoquinoline
The title compound was prepared as described in Example 44.F, using 2- cyclohexanecarbonyl- 1 -(4-hydroxybenzyl)-6-phenylmethoxy- 1 ,2,3 ,4- tetrahydroisoquinoline (0.56 g, 0.12 mmol) to provide the title compound (0.056 g, 68% yield): ES-MS (m z) 567 [M+H]+.
C. 2-Cyclohexanecarbonyl-l - {[4-(2-piperidylethoxy)phenyl]methyl } - 1 ,2,3,4- tetrahydroisoquinolin-6-ol
The title compound was prepared as described in Example 44. G, using 2- cyclohexanecarbonyl- 1 - { [4-(2-piperidylethoxy)phenyl]methyl } -6-phenylmethoxy-
1,2,3,4-tetrahydroisoquinoline (0.056 g) to provide the title compound (0.008 g, 17% yield): 1H NMR (CDC13) 6.5-7.1 (m, 7H), 5.6 (t, 0.5H), 4.9 (t, 0.5H) (amide bond rotamers), 4.7 (m, IH), 4.1 (t , 2H), 3.7 (m, 0.5H), 3.5 (m, 0.5H), 2.7-3.1 (m, 10H), 0.8-
1.9 (m, 16H); ES-MS (m/z) 477 [M+H]+.
EXAMPLE 59
2-(4-FLU0R0PHEN YL } - 1 -[(4-HYDROXYPHEN YL } METHYL]- 1 ,2,3 ,4- TETRAHYDROISOQUINOLIN-6-OL
The title compound was prepared as described in Example 2 using 2-(4- fluorophenyl)-6-methoxy-l-{4-hydroxybenzyl}-l, 2, 3,4-tetrahydroisoquinoline (0.8 g, 2.2 mmol). Purification by column chromatography (SiO2, hexanes/ethylacetate, 2:1) provided the title compound (0.4 g, 57% yield): ES-MS (m/z) 350 [M+H]+.
EXAMPLE 60 1 -[(4-FLUOROPHENYL)METHYL]-2-(4-FLUOROPHENYL)- 1,2,3,4-
TETRAHYDROISOQUINOLIN-6-OL
A. N-{2-[(3-Phenylmethoxy)phenyl]ethyl}-N-(4-fluorophenyl)-2-[2-(4- fluorophenyl)] acetamide The title compound was prepared as described in Example 3. A using (4- fluorophenyl)-{2-[3-(phenylmethoxy)phenyl]ethyl} amine (6.42 g, 20 mmol) and 4- fluorophenylacetyl chloride (3.45 g, 20 mmol) to provide the title compound (9 g, 99% yield): ES-MS (m/z) 458 [M+H]+.
B. l-{4-Fluorobenzyl}-6-phenylmethoxy-2-fluorophenyl-l.2,3,4- tetrahvdroisoquinoline
The title compound was prepared as described in Example 1.D using N- {2-[(3-phenylmethoxy)phenyl]ethyl} -N-(4-fluorophenyl)-2- {2-(4- fluorophenyl} acetamide (9 g, 19.7 mmol). Purification by column chromatography (Siθ2, hexanes/ethylacetate 3: 1) provided the title compound (3.2 g, 36% yield): ES- MS (m/z) 442 [M+H]+.
C l-[(4-Fluorophenyl)methyll-2-(4-fluorophenyl)- 1,2,3,4- tetrahydroisoquinolin-6-ol The title compound was prepared as described in Example 14.D. using 1-
[(4-fluorophenyl)mεthyl]-6-phenylmethoxy-2-fluorophenyl- 1 ,2,3 ,4- tetrahydroisoquinoline (0.2 g, 0.45 mmol). Purification by column chromatography (SiO2, hexanes/ethylacetate, 2: 1) provided the title compound (0.1 g, 62% yield): ES- MS (m/z) 352 [M+H]+.
EXAMPLES 61-134 EXPERIMENTAL PROCEDURE FOR COMBINATORIAL LIBRARY
Reaction Scheme
Scheme for Combinatorial Library (Examples 61 -134)
NaOH, eOH, 0°C
4-Hydroxyphenylacetic acid (100 g, 0.6 mol) and cesium carbonate (250 g) were suspended in 300 mL of anhydrous acetonitrile followed by addition of 1,2- dibromoethane (300 mL). The suspension was brought to reflux for 24 hours in a 2L 3 neck round bottom flask fitted with a mechanical stirrer and reflux condenser then cooled to room temperature. The mixture was diluted to a volume of 2L by addition of ethyl ether and the suspension was filtered. Concentration of the filtrate in vacuo afforded a colorless oil which was purified by vacuum distillation (0.2 mm Hg, 140- 145°C) to give methyl 4-(2-bromoethoxy)-phenylacetate (93.14 g, 60% yield) as a colorless oil. The methyl 4-(2-bromoethoxy)-phenylacetate was taken into methanol (250 mL) and the resulting solution was cooled to 0°C. Sodium hydroxide (29 g) in a minimum of water was added to the methanol solution in portions and the mixture was stirred at 0°C for an additional 30 minutes. The solution was warmed to room temperature then concentrated to a white solid. The residue was taken into water and the solution washed once with ethyl ether. The aqueous solution was then acidified to pH 1 by addition of concentrated aqueous hydrochloric acid to give a thick suspension. Filtration and drying afforded 4-(2-bromoethoxy)-phenylacεtic acid (86 g, 97% yield) as a colorless solid. The 4-(2-bromoethoxy)-phenylacetic acid (50 g) was taken into thionyl chloride (70 mL) and brought to reflux under an atmosphere of nitrogen for 2 hours. Fractional vacuum distillation (0.2 mm Hg, 139-140°C) afforded 4-(2- bromoethoxy)phenylacεtyl chloride (46. Og, 86% yield) as a colorless oil that quickly crystallized on cooling. Η NMR (CDC13) 6.95, 6.76, 6.60 (m, 11 H, Ar-H), 4.68 (m, IH), 4.24 (m, 2 H), 3.80 (m, IH), 3.41-3.63 (m, 3H), 3.07 (m, IH), 2.87 (m, 2H), 2.61 (m, IH); ES-MS (m/z) 458 [M+H]+. B. l-[4-(2-Bromoethoxy)benzyl]-2-(4-fluorophenyl)-l,2,3.4-tetrahydroisoquinolin- 6-ol
N-(4-Fluorophenyl)-4-benzyloxyphenethylaminε hydrochloride (19.1g,
53.4 mmol) was suspended in dichloromethanε (100 mL) followεd by addition of pyridinε (1 1 mL, 133.5 mmol) and thε rεsulting solution was cooled to 0°C. 4-(2- Bromoethoxy)-phenylacetyl chloride (16.3 g, 58.7 mmol) in dichloromethane (50 mL) was added dropwise to the amine solution over 30 minutes followed by warming the
mixmre to room temperature. The solution was washed with 1.0 N aqueous hydrochloric acid, dried over anhydrous MgSO then filtered. The filtrate was concentrated to afford 34.2 g of a yellow oil. The oil was taken into anhydrous acetontrilε (150 mL) and phosphorous oxychloridε (75 mL) was added to the solution. The mixture was brought to reflux under an atmosphere of nitrogen for 12 hours then cooled to room temperature and concentrated to an oil. The residue was taken into ethyl acetatε and thε solution cooled to 0°C followed by careful quenching by slow addition cf one volumε εquivalent of water. The organic layer was washed with additional water then with saturated aqueous sodium chloride. The organic layer was then concentrated to an oil and taken into dichloromethanε and methanol (1 :1 , 250 mL). The resulting solution was cooled to 0°C and sodium borohydride (3.9 g) was addεd in portions over 15 minutes. The mixture was warmed to room temperature and stirred an additional 15 minutes, during which time the evolution of hydrogen gas ceased. The reaction mixmre was concentrated and partitioned with ethyl acetate and water. The organic layer was washed with additional water then with saturated aqueous sodium chloride and dried over anhydrous MgSO . Filtration and concentration afforded a yellow oil. The oil was taken into 30%> hydrogen bromide in acetic acid (175 mL) and the solution was stirred for 15 minutes then partitionεd with ethyl acetate (500 mL) and water (500 mL). Solid sodium hydrogen carbonate (75 g) was added in portions and the organic layer was washed 3x with additional water then with saturated aqueous sodium chloride and dried over anhydrous MgSO4. Filtration, concentration and purification by column chromatography (Siθ2) afforded l-[4-(2-bromoethoxy)benzyl]-2-(4-fluorophenyl)- l,2,3,4-tetrahydroisoquinolin-6-ol as a yellow oil (8.75 g). !H NMR (CDC ) 6.95, 6.76, 6.60 (m, 1 1 H, Ar-H), 4.68 (m, 1 H), 4.24 (m, 2 H), 3.80 (m, IH), 3.41-3.63 (m, 3 H), 3.07 (m, 1 H), 2.87 (m, 2H), 2.61( m, IH); ES-MS m/z 458 [M+FI]+.
C. Genεral Procedure for Alkylations of l-[4-(2-Bromoethoxy)benzyl]-2-(4- fluorophenyl)-l,2,3,4-tetrahydroisoquinolin-6-ol
A 16 mm x 100 mm screw cap tube was charged with the bromide (75 mg, 0.164 mmol) and THF (1 mL). The appropriate secondary amine (1.0 mmol, 6.1 equiv) was added and the tube was sealεd. The reaction was heated at 70 °C for 24 hours with magnetic stirring. The reaction was cooled to 23 °C, taken up in
acetonitrile/water (1 :1, 2 mL) and purified by preparative HPLC (C-18 column, 10%- 90%) acetonitrile in water, with 0.1% HCl). The product was isolated and the solvents were removed by lyophilization. All final products were characterized by ES-MS.
D. Representative Compounds
By the procedures set forth above, the compounds listed in Table 2 were prepared.
Table 2 Representative Compounds
EXAMPLE 135 -(4-FLUOROPHENYL)-6-PHENYLMETHOXY- 1 - {4-[( 1 -PIPERIDYL)PROP-2-ENYL]BENZYL} ■
1 ,2,3,4-TETRAHYDROISOQUINOLINE
Scheme for Example 135 and 136 (Carbon Sidechains)
Example 135
Example 136
To a solution of l-(4-bromobenzyl)-6-phenylmethoxy-2-phenyl- 1,2,3,4- tetrahydroisoquinoline (0.502 g, 1 mmol) in anh acetonitrile (10 mL) under an atmosphεre of nitrogen is added Pd(dba)3 (0.092 g, 0.1 mmol), tri-o-tolylphosphine (0.122 g, 0.4 mmol), TEA (3 mL) and piperidineallyl (0.25 g, 2 mmol). The reaction was heated at 100°C overnight, then cooled to room temperature. The reaction mixture was quenched with water and a 5% HCl solution was added. The crude product was extracted with ethylacetate, washed with brine, dried over MgSO and purified by column chrorr-atography (Siθ2, GK C MeOH, 95:5) to provide tlte title compound (0.113 g, 21% yield): ES-MS (m/z) 547 [M+H]+.
EXAMPLE 136
2-(4-FLUOROPHENYL)- 1 - {4-[( 1 -PIPERIDYL)PROPYL]BENZYL} - 1 ,2,3,4-
TETRAHYDROISOQUINOLIN-6-OL
The title compound was prepared as described in Example 44. G using 2-
(4-fluorophεnyl)- 1 - {4-[( 1 -piperidyl)prop-2-enyl]benzyl} - 1 ,2,3,4-tetrahydroisoquinolin- 6-ol (0.10 g, 0.18 mmol) to provide the title compound (0.009 g, 1 1% yield): ES-MS (m/z) 459 [M+H]+.
EXAMPLE 137 2-(4-FLUOROPHENYL)-5-METHOXY- 1 - {4-[(2-PIPERIDYL)ETHOXY]BENZYL} ISOINDOLINΈ
/55137
Reaction Scheme
Scheme for Example 137, 138
Example 138
A. 2-(4-Fluorophenyl)-3-(4-hydroxybenzyl)-6-methoxyisoindolin-l-one
To a solution of triphenyl(5-methoxy-3-oxo-l,3-dihydro-isobεnzofuran- l-yl)phosphomium bromidε (10.00 g, 19.8 mmol) (Sakamoto et al., Chem. Pharm. Bull 31, 2698-2707, 1983) and 4-benzyloxybenzaldehyde (10.074 g, 24.0 mmol) in CH2C12 (100 mL) at -10 °C was added triethylamine (4 mL). After stirring at room temperature for 2 hours, the solvent was evaporated. To the residuε was added ethyl ether to provide a mixture of (E)- and (Z)-6-methoxy-3-{[4-
phenylmethoxy)phenyl]methylene}isobenzofuran-l-one (4.56 g, 64% yield); ES-MS (m/z) 359 [M+H]+. A solution of (E)- and (Z)-6-methoxy-3-{[4- phenylmethoxy)phenyl]methylene}isobenzofuran-l-one (2.00 g, 5.58 mmol), 4- fluoroaniline (4 mL) and acetic acid (3 mL) in 1,4-dioxane (30 mL) was prepared and heated at 120 °C overnight. The reaction was quenched with ethyl acetate and washed with 5% hydrochloride solution, then saturated sodium bicarbonate solution. The organic layer was dried over MgSO4, filtered, and concentrated. The residue was purified by chromatography (SiO2, 15-50% ethyl acetatε/hexane) to provide a mixture of (E)- and (Z)-6-methoxy-3-{[4-phenylmεthoxy)phεnyl]methylene}isoindolin-l-one (1.529 g, 61% yield): ES-MS (m/z) 452 [M+H]+. A mixture of the (E)- and (Z)-6- methoxy-3-{[4-phenylmethoxy)phenyl]mεthylene}isoindolin-l-one (1.40 g, 3.1 mmol) was dissolved in methanol (10 mL) and tetrahydrofuran (10 mL), then palladium (10% wt. on activated carbon, 0.20 g) was added and thε reaction was stirred under hydrogen overnight. The mixture was filtered through celite, concentrated, and washed with ethyl ether and CH2C12 to provide the title compound (1.094 g, 97%> yield): IH NMR (CDC13) 7.56 (m, 2H), 7.30 (d, IH), 7.18 (t, 2H), 7.07 (dd, IH), 7.02 (d, IH), 6.60-6.67 (m, 4H), 5.29 (dd, IH), 5.19 (s, IH), 3.84 (s, 3H), 3.24 (dd, IH), 2.78 (dd, IH); ES-MS (m/z) 364 [M+H]+.
B. 2-(4-Fluorophenyl)-6-methoxy-3- {4-[(2-pipεridyl)εthoxy]benzyl}isoindolin-l- one
The tide compound was prepared as described in Example 3.D, using 2-
(4-Fluorophenyl)-3-[4-hydroxyphenyl)methyl]-6-methoxyisoindolin-l-one (1.05 g, 2.89 mmol) to provide the title compound (1.097 g, 80% yield): IH NMR (CDC13) 7.56 (m,
2H), 7.30 (d, IH), 7.18 (t, 2H), 7.06 (dd, IH), 6.99 (d, IH), 6.70 (s, 4H), 5.30 (dd, IH), 4.04 (t, 2H), 3.85 (s, 3H), 3.25 (dd, IH), 2.76 (t and m, 3H), 2.51 (m, 4H), 1.61 (m, 4H),
1.45 (m, 2H); ES-MS (m/z) 475 [M+H]+.
C. 2-(4-Fluorophenyl)-5-methoxy-l-{4-[(2-pipεridyl)εthoxy]bεnzyl}isoindo]ine
To a solution of 2-(4-fluoroρhenyl)-6-methoxy-3-{4-[(2- piperidyl)ethoxy]benzyl}isoindolin-l-one (0.50 g, 1.05 mmol) in tetrahydrofuran (10 mL) under nitrogen was added a 1.5 M solution of borane-tetrahydrofuran complex in tetrahydrofuran (2 mL, 3 mmol). After heating at reflux for 5 hours, the reaction was
cooled to room temperature, 6 N HCl solution (6 mL) was added, and the reaction was stirred for 1 hour at room temperature. The mixture was basified with a saturated sodium bicarbonate solution and extracted with CH2CI2. The organic layer was dried over MgSO , filtεred, and concentrated. The residuε was thεn purifiεd by chromatography (SiO2, 20-30% ethyl acetate/hεxane) to provide the title compound (0.297 g, 61% yield): IH NMR (CDCI3) 7.05 (t, 2H), 6.91 (d, IH), 6.78 (dd, IH), 6.61- 6.72 (m, 7H), 5.24 (m, IH), 4.30-4.41 (m, 3H), 4.15 (dd, IH), 3.80 (s, 3H), 3.17 (t, 2H), 2.98-3.10 (m, 4H), 2.91 (m, 2H), 1.81 (m, 4H), 1.56 (m, 2H); ES-MS (m/z) 461 [M+Hf.
EXAMPLE 138
2-(4-FLUOROPHENYL)- 1 -(4-HYDROXYBENZYL)ISOINDOLΓN-5-OL
To a solution of 2-(4-fluorophenyl)-5-methoxy-l-{4-[(2- pipεridyl)εthoxy]bεnzyl}isoindolinε (0.14 g, 0.3 mmol) in CH2CI2 (8 mL) undεr nitrogen at -10 °C was added a 1.0 M solution of boron tribromide in CH2C12 (0.6 mL, 0.6 mmol) dropwise. After stirring at -10 °C for 1 hour, the reaction was quenched with ice and saturated sodium bicarbonate, then extracted with methylenε choride. The organic layer was dried over MgSO , filtered, and concentrated. The residue was then purified by HPLC (C-18 column, 10-100% acetonitrile/watεr with 0.1% trifluoroacetic acid) to provide the title compound (0.084 g, 84% yield): IH NMR (DMSO-d6) 7.04 (t, 2H), 6.88 (d, IH), 6.69 (dd, IH), 6.61-6.65 (m, 5H), 6.56 (d, IH), 5.21 (m, IH), 4.67 (s, IH), 4.51 (s, IH), 4.29 (d IH), 4.10 (dd, IH), 3.00-3.14 (m. 2H); ES-MS (m/z) 336 [M+H]+.
55137
EXAMPLE 139 SYNTHESIS OF 2-(4-FLUOROPHENYL)- 1 - {4-[(2-PIPERIDYL)ETHOXY]BENZOYL} - 1 ,2,3,4-
TETRAHYDROISOQUINOLIN-6-OL
Reaction Scheme
Scheme for Example 139
II
Example 139
A. l-[4-(2-Bromoethoxy)phenyl]ethanone
A mixmre of 1 -(hydroxyphenyl)ethanone (2.72 g, 20.0 mmol), 1,2- dibromoethane (7.676 g, 40.0 mmol), and potassium carbonate (5.52 g, 40 mmol) in dried dimethylformamidε (40 mL) was heated at 50 °C overnight. The reaction was quenched with water and extracted with ethyl acetate. The organic layer was dried over MgSO4, filtered, concentratεd, and purified by column chromatography (Siθ2, 20-70% ethyl acetate/hexane) to provide the title compound (1.91 g, 39%> yield): 1H NMR (CDC13) 7.95 (t, 2H), 6.95 (t, 2H), 4.36 (t, 2H), 3.67 (t, 2H), 2.57 (s, 3H); ES-MS (m/z) 243 [M+Hf. B. [4-(2-Bromoethoxy)phenyl]glyoxal
A suspension of selenium dioxide (0.821 g, 7.4 mmol) in 1,4-dioxane
(40 mL) and watεr (3 mL) was hεated at 55 °C until selenium dioxide was dissolved.
To the solution was added l-[4-(2-bromoethoxy)phεnyl]εthanonε (1.80 g, 7.4 mmol), and the reaction was heated to reflux for 4 hours. The reaction was filtered, concentrated, and purified by column chromatography (SiO2, 50?/ό ethyl acetate/hexanε) to providε the title compound (1.853 g, 97% yield): ES-MS (m/z) 257 [M+H]".
C. 1 - 4-(2-Bromethoxy)benzoyl]-2-(4-fluorophenyl)-6-(phenylmεthoxy)- 1.2,3,4- tetrahydroisoquinoline
To a solution of (4-fluorophenyl) {2-[3- (phenylmethoxy)phenyl] ethyl} amine (0.643 g, 2.0 mmol) and [4-(2- bromoethoxy)phenyl]glyoxal (0.617 g, 2.4 mmol) was added trifluoroacetic acid (0.342 g, 3.0 mmol). Thε reaction stirred at room temperature for 4 hours. The reaction was quenched with saturated sodium bicarbonate and extracted with ethyl acetate. The organic layer was dried over MgSO4, filtered, concentrated, and purified by column chromatography (SiO2, 20% ethyl acetate/hexane) to provide the title compound (0.879 g, 78% yield): Η NMR (CDC13) 8.00 (d, 2H), 7.40 (m, 4H), 7.18 (m, IH), 7.07 (d, IH), 6.79-6.92 (m, 8H), 5.85 (s, IH), 5.02 (s, 2H), 4.33 (t, 2H), 3.71 (m, IH), 3.64 (t, 2H), 3.47 (m, IH), 3.07 (m, IH), 2.87 (m, IH); ES-MS (m/z) 560 [M+H]+.
D. 2-(4-Fluorophenyl)-l-{4-[(2-piperidyl)ethoxy]benzoyl}-6-(phenylmethoxy)- 1.2,3,4-tεtrahydroisoquinolinε
A solution of l-[4-(2-bromεthoxy)bεnzoyl]-2-(4-fluorophenyl)-6-
(phenylmethoxy)- 1,2,3,4-tetrahydroisoquinoline (0.80 g, 1.43 mmol) and piperidine (0.86 g, 10.1 mmol) in dimεthylformamide was stirred at room temperature for 3 hours.
The reaction was quenched with brine and extracted with ethyl acetate. The organic layer was dried over MgSO , filtered, concentrated, and purified by chromatography
(Siθ2, ethyl acetate and 3-5% methanol/ethyl acetate) to provide thε titlε compound
(0.594 g, 74% yield): 1H NMR (CDC13) 8.00 (m, 2H), 7.40 (m, 4H), 6.79-6.92 (m, 10H), 5.87 (s, IH), 5.02 (s, 2H), 4.15 (t, 2H), 3.72 (m, IH), 3.48 (m, IH), 3.07 (m, IH),
2.79 (t and m, 3H), 2.51 (m, 4H), 1.61 (m, 4H), 1.46 (m, 2H); ES-MS (m z) 565
[M+H]+.
E. 2 -(4-Fluorophenyl)- 1 - {4-[(2-piperidyl)ethoxy]benzoyl } - 1 ,2,3 ,4- tetr.ahydroisoquinolin-6-ol The title compound was prepared as described in Example 14.D, using 2-
(4-fluorophenyl)- 1 - {4-[(2-piperidyl)ethoxy]bεnzoyl } -6-(phenylmethoxy)- 1 ,2,3 ,4- tetrahydroisoquinoline (0.35 g, 0.62 mmol) to provide the title compound (0.039 g, 13% yield): Η NMR (CDC13) 7.96 (d, 2H), 6.79-7.00 (m, 7H), 6.56-6.63 (m, 2H), 5.83 (s, IH), 4.16 (t, 2H), 3.69 (m, IH), 3.44 (m, IH), 3.04 (m IH), 2.84 (t, 2H), 2.79 (m, IH), 2.59 (m, 4H), 1.64 (m, 4H), 1.46 (m, 2H); ES-MS (m/z) 475 [M+H]+.
EXAMPLE 140 ER-SELECTIVITY IN U2OS OSTEOSARCOMA CELLS Human U2OS osteosarcoma cells (ATCC) were stably transfected with expression vectors for human full-length ER-α or ER-β, respectively, using standard molecular biology techniques. Stable subclones were generatεd that εxprεssεd high levels of ER-α or ER-β mRNA. The expression of ER-α and ER-β was confirmed using RNase protection analysis. The parental U2OS cells did not express any measurable amounts of eithεr ER-α or ER-β.
Cells were plated into 96-well platεs at a density of 8000 cells per well in phenol red-free media with charcoal-stripped fetal calf serum. Twεnty-four hours
/55137
later, cells were either treated with vehicle (0.2%o DMSO) or test compound at the concentrations indicated (in 0.2% DMSO). Thirty minutes later cells were stimulated with 10 ng/ml IL-lβ and 10 ng/ml TNF-α. Twenty- four hours later the media supernatant was analyzed for cytokine production (IL-6) using commercially available ELISA kits following the manufacturer's instructions. Cytokine production in the presence of vehicle (0.2% DMSO) was set to 100%.
Results of this assay are set forth in Table 4 for a number of representative compounds of this invention, as well as for the prior art test compounds. In this table, activity is expressed as IC5o calculated by 50% inhibition relativε to DMSO control (100%). In this εxpεriment, the prior art test compounds were 17-β- Estradiol, Raloxifene Hydrochloride, 4-Hydroxy-Tamoxifen, and the following compound disclosed in published PCT WO 96/21656 (referred to herein as "Compound A"):
Compound A
Table 4 Effect of Representative SERMs on Cytokines
Refεrring to the above table, representative compounds of this invention showed specificity for ER-β over ER-α, while the prior art compounds (with the exception of 17-β-Estradiol) were selective for ER-α over ER-β. In this regard, preferred components of this invention have an IC o of less than lμM, and more prefεrably 500nM or less.
EXAMPLE 141 ER-SELECTIVITY IN BREAST CANCER CELLS
Tamoxifen resistant breast cancer cells, in this case LCCl and LCC2 cells (R. Clarke, Georgεtown University), were plated in 96-well dishes at 5000 cells per well in phenol-red free medium containing 5% charcoal-stripped serum. Threε hours later, test compounds were prepared by serial dilution and added to the cells to yield a final concentration of 0.2%> DMSO. Compounds were prepared fresh and added daily for 4 days with media change after 48 hours. On the fifth day, [3H] -thymidine (2.5 μCi/ml) was added to each well of the 96-well dish and the plate incubated at 37°C for 6 hours. At the end of the incubation, the cells were lysed and thε [3H]-thymidinε incoφorated determinεd using a scintillation counter.
The results of this experiment for Compound 102 (Example No. 5) of this invention are set forth in Figure 1A for LCCl cells, and Figure IB for LCC2 cells.
This experiment evidences that representative compounds of this invention are effective in Tamoxifen-rεsistant breast cancer cell lines.
It will be appreciated that, although specific embodiments of the invention have been described herein for purpose of illustration, various modifications may be made without departing from the spirit and scope of the invention. Accordingly, the invention is not limited except as by the appended claims.
Claims
A compound having the structure:
A, B and C are indepεndently CH, CR or N;
D is -(CH2 or -(CH2)„C(=O)(CH2)„-;
Ri represents one or two substituents independently selected from -X-Y;
R2 is Cι-8alkyl, C6-i2aryl, C7-i2aralkyl, -C(=O)R5, a five- or six-membered heterocycle or heterocyclealkyl containing up to two heteroatoms selεctεd from O, NRc and S(O)9, or a bicyclic ring system contain a five- or six-membered heterocycle fused to phenyl, whεrein each of the above groups are optionally substituted with one to three substituents independently selected from -X-Y or R^ and
R3 is hydrogen, -Re, 
-(CH2),C(=O)NR6R7, -(CH2)JC(=O)NR6(CH2)„C(-O)R7R8, 
-(CH2).OR6, -(CH2)sSO(?R6 or -(CH2),SO2NR6R7; and wherein
R-t is at each occurrence independently halogen, hydroxy, carboxy, Cι.6alkyl, Cι- alkoxy, C haloalkyl, Cι--ιacyloxy, Cι- hio, Cι- alkylsulfinyl, Ci- alkylsulfonyl, (hydroxy)Cι- alkyl, C6-i2aryl, C7-ι2aralkyl, -C(=O)OH, - C(=O)OR, -OC(=O)R, -C(=O)NHR, -C(=O)NRR, -C(=O)NHOR, - SO2NHR, -NHSO2R, -CN, -NO2. -NH2, C,. alkylamino, C dialkylamino, -NHC(=O)R, NHC(=0)(CH2)5(five- or six- membered heterocycle), a five- or six-membered heterocycle, or a five- or six-membered heterocycle fused to phenyl; R5, R , R7 and R8 are at each occurrence independεntly hydrogen, Cι-8alkyl, C6-i2aryl, C7-i2 ralkyl, or a five- or six-membered heterocycle or heterocyclealkyl containing up to two heteroatoms selected from O, N c and S(O)?, wherein each of the above groups are optionally substituted with one to three substituents independently selεcted from 
X is at each occurrence independently a direct bond;
-(CH2)nZ(CH2)m-;
-O(CH2)nZ(CH2)m-;
-S(CH2)nZ(CH2)m-;
-NRc(CH2)nZ(CH2)m-;
-O(CH2)nCRaRb-;
-NRc(CH2)nCRaRb-;
-OCHRcCHRd-; or
-SCHRcCHRj-; Y is at each occurrence independently halogen;
-R.; -NReRr; ftr
1 , optionally fused on adjacent carbon atoms with one or two phenyl or cycloalkyl rings, and with each carbon optionally and independεntly substitutεd with carbonyl or with onε or two substituents independently selected from R4, with any two j substituents on a single carbon atom optionally being taken togethεr to form a five- or six-membered heterocycle, and with each nitrogen atom optionally and independently substituted with R4, wherein W is -NR.-, -O-, -S- or -CReRf-; or a bridged or fused C -ι2bicyclic amine optionally substituted with one to three substituents independεntly selected from *; or where -X-Y is
Z is CH2, CH-CH, C≡C, O, NRc, S(O)q, C( )), C(OH)Rc, C(=O)NRc,NRcC(=O), C(=O)NRc, NRcC(O) or \_/ ;
G is O, S or NRe; n and m are at each occurrence independently 0, 1, 2 or 3; p is at each occurrence independently 1, 2 or 3; q is at each occurrence independently 0, 1 or 2; r is at each occurrence indepεndently 1, 2, 3, 4 or 5; s is at each occurrence indepεndently 0, 1, 2, 3 or 4;
R is at each occurrence independently Cι-6alkyl;
Ra and R, are at each occurrence independently Cj-8alkyl or taken together form a C3-8cyclic alkyl;
Re and Rj are at each occurrence independently hydrogen or Cι- alkyl; and
Re and Rf are at each occurrence indεpεndεntly hydrogen, C6-12aryl, Cι-8alkyl, C7-i2aralkyl, a five- or six-membered heterocycle, or a five- or six- membered heterocycle fused to phenyl; or wherεin Re or Rf form a 3-8 mεmbεred nitrogen-containing hetεrocyclic alkyl with Ra or R^; and wherein each Re and Rf are optionally substituted with up to three substituents independently selected from t.
2. The compound of claim 1 wherein a is 1.
3. The compound of claim 1 wherein a is 0.
4. The compound of claim 1 wherein a is 2.
5. The compound of claim 1 wherein A and B are CH.
6. The compound of claim 1 wherein A is CH and B is CR.
7. The compound of claim 1 wherein A is CH and B is nitrogen
8. The compound of claim 1 wherein A and B are nitrogen.
9. The compound of claim 1 wherein C is nitrogen.
10. The compound of claim 1 wherein C is CH or CR.
11. The compound of claim 1 wherein D is -(CH2)r-.
12. The compound of claim 1 1 wherien r is 1.
13. The compound of claim 1 wherein D is 
14. The compound of claim 13 wherein n and m are both 0.
15. The compound of claim 1 wherein A and B are CH, C is N and D is
-CH,-.
16. The compound of claim 15 wherein a is 1 and having the structure: 
17. The compound of claim 15 wherein a is 0 and having the strucmre:
18. The compound of claim 15 wherein a is 2 and having the structure:
19. The compound of claim 16 having the structure:
20. The compound of claim 19 having the structure:
21. The compound of claim 19 having the structure:
22. The compound of claim 19 wherein R is Cι-8alkyl.
The compound of claim 1 wherein A is nitrogen, B is CH, C is nitrogen and D is -CH2
24. The compound of claim 23 wherein a is 1 having the structure: 
25. The compound of claim 24 having the structure:
26. The compound of claim 1 wherein A and B are N, C is N, and D is
-CH2
27. The compound of claim 1 wherein A, B and C are CH, and D is -CH2-
28. The compound of claim 1 wherein Ri represents a single -X-Y substituent.
29. The compound of claim 28 wherein X is -(CH2)nZ(CH2)n
30. The compound of claim 29 wherein n is 0.
31. The compound of claim 30 wherein Z is oxygen.
32. The compound of claim 28 wherein X is a direct bond and Y is -Re or
-NReRf.
33. A pharmaceutical composition comprising a compound of claim 1 and a pharmaceutically acceptable carrier or diluent.
34. A method for modulating ER-β in a cell expressing ER-β, comprising contacting the cell with an effective amount of a compound of claim 1.
35. The method of claim 32 wherein the cell preferentially expresses ER-β over ER-α.
36. The method of claim 35 wherein the cell is of bone, bladder, uterus, ovary, prostate, testis, epididymis, gastrointestinal tract, kidney, breast, eye, heart, vessεl wall, immune system, lung, pituitary, hippocampus or hypothalamus cell.
37. A method for modulating ER-β in tissue expressing ER-β, comprising contacting the tissue with an effective amount of a compound of claim 1.
38. The method of claim 37 wherein the tissue preferentially expresses ER- β over ER-α.
39. The method of claim 38 wherein the tissue is tissue of bone, bladder, uterus, ovary, prostate, testis, epididymis, gastrointestinal (GI) tract, kidney, breast, eye, heart, vessel wall, immune system, lung, pituitary, hippocampus or hypothalamus.
40. A method for treating an estrogen-related condition, comprising administering to an animal in need thereof an effective amount of a pharmaceutical composition of claim 33.
41. The method of claim 40 wherein the εstrogεn-rεlatεd condition is breast cancer, osteoporosis, endometriosis, cardiovascular disease, hypercholestεrolemia, prostatic hypertrophy, prostatic carcinomas, obesity, hot flashes, skin effects, mood swings, memory loss, prostate cancer, menopausal syndromes, type-II diabetes, Alzheimer's disease, urinary incontinence, GI tract conditions, spermatogenesis, vascular protection after injury, endometriosis, learning and memory, CNS effects, plasma lipid levels, acne, hirsutism, solid cancers, multiple myeloma, lymphoma, hairloss, cataracts, namral hormonal imbalances, or adverse reproductive effects associated with exposure to environmental chemicals.
42. A method for inhibiting a cytokine in an animal in need thereof, comprising administering to the animal an effective amount of a compound of claim 1.
42. The method of claim 42 wherein the cytokine is IL-6
43. The method of claim 42 wherein the cytokine is GM-CSF.
44. A method for treating cancer associated with IL-6 in an animal in need thereof, comprising administering to the animal an effective amount of a compound of claim 1.
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| CA002367895A CA2367895A1 (en) | 1999-03-17 | 2000-03-17 | Compounds and methods for modulation of estrogen receptors |
| EP00921397A EP1163225A1 (en) | 1999-03-17 | 2000-03-17 | Compounds and methods for modulation of estrogen receptors |
| AU41725/00A AU766648B2 (en) | 1999-03-17 | 2000-03-17 | Compounds and methods for modulation of estrogen receptors |
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| US24090999P | 1999-03-17 | 1999-03-17 | |
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| US (3) | US6436923B1 (en) |
| EP (1) | EP1163225A1 (en) |
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| AU (1) | AU766648B2 (en) |
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Also Published As
| Publication number | Publication date |
|---|---|
| AU4172500A (en) | 2000-10-04 |
| US7435729B2 (en) | 2008-10-14 |
| US20050004360A1 (en) | 2005-01-06 |
| WO2000055137A8 (en) | 2001-07-05 |
| US6436923B1 (en) | 2002-08-20 |
| US20030087901A1 (en) | 2003-05-08 |
| CA2367895A1 (en) | 2000-09-21 |
| EP1163225A1 (en) | 2001-12-19 |
| US6686351B2 (en) | 2004-02-03 |
| AU766648B2 (en) | 2003-10-23 |
| JP2003521468A (en) | 2003-07-15 |
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