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【结 构 式】

【药物名称】NNC-45-0781

【化学名称】(-)-3(S)-Phenyl-4(R)-[4-[2-(1-pyrrolidinyl)ethoxy]phenyl]-3,4-dihydro-2H-1-benzopyran-7-ol

【CA登记号】207277-66-5

【 分 子 式 】C27H29NO3

【 分 子 量 】415.53708

【开发单位】Novo Nordisk (Originator)

【药理作用】Bone Diseases, Treatment of, Cognition Disorders, Treatment of, ENDOCRINE DRUGS, Gynecological Disorders, Treatment of , METABOLIC DRUGS, NEUROLOGIC DRUGS, Treatment of Osteoporosis, Treatment of Postmenopausal Syndrome , Selective Estrogen Receptor Modulators (SERM)

合成路线1

Coumarin (III) was prepared by condensation of benzophenone (I) with phenylacetic acid (II) in the presence of Ac2O and Et3N. Reduction of the lactone function of (III) with LiAlH4, followed by acidic treatment furnished diaryl chromene (IV). Subsequent hydrogenation of (IV) over Pd/C gave rise to the racemic cis chromane (V), which was O-alkylated with 1-(2-chloroethyl) pyrrolidine (VI) producing the corresponding (pyrrolidinyl)ethoxy derivative. Resolution by means of active ditoluoyl tartaric acid yielded the desired (-)-enantiomer (VII). Finally, cleavage of the methoxy group using pyridine hydrochloride at 150 C provided the title compound.

1 Bury, P.S.; et al.; Synthesis and pharmacological evaluation of novel cis-3,4-diaryl-hydroxychromanes as high affinity partial agonists for the estrogen receptor. Bioorg Med Chem 2002, 10, 1, 125.
2 Jacobsen, P.; Treppendahl, S.; Stanley Bury, P.; Kanstrup, A.; Brown Christiansen, L. (Novo Nordisk A/S); Novel cis-3,4-chroman derivs. useful in the prevention or treatment of estrogen related diseases or syndromes. EP 0937060; WO 9818776 .
3 Jacobsen, P.; Treppendahl, S.; Stanley Bury, P.; Kanstrup, A.; Brown Christiansen, L. (Novo Nordisk A/S); Novel (-)-enantiomers of cis-3,4-chroman derivs. useful in the prevention or treatment of estrogen related diseases or syndromes. EP 0937057; WO 9818771 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 35211 (2-hydroxy-4-methoxyphenyl)(4-hydroxyphenyl)methanone C14H12O4 详情 详情
(II) 16148 Benzeneacetic acid; 2-Phenylacetic acid; Phenyl Acetic Acid 103-82-2 C8H8O2 详情 详情
(III) 35212 4-(7-methoxy-2-oxo-3-phenyl-2H-chromen-4-yl)phenyl acetate C24H18O5 详情 详情
(IV) 35213 4-(7-methoxy-3-phenyl-2H-chromen-4-yl)phenol C22H18O3 详情 详情
(V) 35214 4-[(3S,4R)-7-methoxy-3-phenyl-3,4-dihydro-2H-chromen-4-yl]phenol C22H20O3 详情 详情
(VI) 33922 1-(2-Chloroethyl)pyrrolidine; N-(2-Chloroethyl)pyrrolidine C6H12ClN 详情 详情
(VII) 35215 1-(2-[4-[(3S,4R)-7-methoxy-3-phenyl-3,4-dihydro-2H-chromen-4-yl]phenoxy]ethyl)pyrrolidine; 4-[(3S,4R)-7-methoxy-3-phenyl-3,4-dihydro-2H-chromen-4-yl]phenyl 2-(1-pyrrolidinyl)ethyl ether C28H31NO3 详情 详情
Extended Information