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【结 构 式】

【药物名称】

【化学名称】4-[5-(4-Chlorophenyl)-3-(3'-methoxybiphenyl-4-yl)-1H-pyrrol-2-yl]pyridine

【CA登记号】

【 分 子 式 】C28H21ClN2O

【 分 子 量 】436.94537

【开发单位】Merck & Co. (Originator)

【药理作用】Antidiabetic Drugs, ENDOCRINE DRUGS, Glucagon Antagonists

合成路线1

The alkylation of 4-(dimethoxymethyl)pyridine (I) with 4-bromobenzyl bromide (II) in the presence of n-butyllithium, followed by ketal hydrolysis with formic acid provided the diaryl ethanone (III). Further alkylation of (III) with 4-chlorophenacyl bromide (IV) employing sodium hexamethyldisilazide yielded diketone (V), which was cyclized in the presence of ammonium acetate in boiling AcOH to produce pyrrole (VI). Finally, Suzuki coupling of (VI) with 3-methoxybenzeneboronic acid (VII) by means of Pd(PPh3)4 furnished the title compound.

1 McMillan, M.; Cudaback, E.; Misra-Press, A.; et al.; Synthesis and biological studies of a novel inhibitor of NF-kappaB. 217th ACS Natl Meet (March 21 1999, Anaheim) 1999, Abst MEDI 213.
2 de Laszlo, S.E.; Kim, D.; Chang, L.L.; Mantlo, N.B. (Merck & Co., Inc.); Substd. pyridyl pyrroles, compsns. containing such cpds. and methods of use. US 5776954 .
3 De Laszlo, S.E.; Chang, L.L.; Kim, D.; Mantlo, N.B. (Merck & Co., Inc.); Substd. pyridyl pyrroles, compsns. containing such cpds. and methods of use. EP 0859771; JP 1999514651; WO 9716442 .
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) 29418 4-(dimethoxymethyl)pyridinemethoxy(4-pyridinyl)methyl methyl ether C8H11NO2 详情 详情
(II) 16109 1-bromo-4-(bromomethyl)benzene; 4-Bromobenzyl bromide 589-15-1 C7H6Br2 详情 详情
(III) 29423 2-(4-bromophenyl)-1-(4-pyridinyl)-1-ethanone C13H10BrNO 详情 详情
(IV) 16720 2-bromo-1-(4-chlorophenyl)-1-ethanone; 2-Bromo-4'-chloroacetophenone 536-38-9 C8H6BrClO 详情 详情
(V) 29424 2-(4-bromophenyl)-4-(4-chlorophenyl)-1-(4-pyridinyl)-1,4-butanedione C21H15BrClNO2 详情 详情
(VI) 29425 4-[3-(4-bromophenyl)-5-(4-chlorophenyl)-1H-pyrrol-2-yl]pyridine C21H14BrClN2 详情 详情
(VII) 29426 3-methoxyphenylboronic acid 10365-98-7 C7H9BO3 详情 详情
Extended Information