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【结 构 式】

【分子编号】53284

【品名】8-bromo-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-one

【CA登记号】n/a

【 分 子 式 】C14H10BrNO

【 分 子 量 】288.14354

【元素组成】C 58.36% H 3.5% Br 27.73% N 4.86% O 5.55%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(I)

The known tricyclic bromide (I) was converted to the nitrile (II) by treatment with CuCN and NaCN. Addition of the Grignard reagent (IV), prepared from 4-chloro-1-methylpiperidine (III), to the tricyclic ketone (II) furnished the tertiary alcohol (V). This was finally dehydrated to the target piperidylidene derivative upon heating in the presence of SOCl2.

1 Honda, H.; Mizuno, H.; Mogi, K.; Ito, Y.; Kaneko, Y.; Taido, N.; Sato, S.; Kuraishi, T. (SSP Co., Ltd.); Novel benzo[5,6]cyclohepta[1,2-b]pyridine derivs. and antiallergic agents comprising same. EP 0495484; JP 1993059040; US 5231101 .
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) 53284 8-bromo-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-one n/a C14H10BrNO 详情 详情
(II) 53585 4-[(5-bromopentyl)oxy]-1,1'-biphenyl; [1,1'-biphenyl]-4-yl 5-bromopentyl ether n/a C17H19BrO 详情 详情
(III) 20949 4-Chloro-1-methylpiperidine; 4-Chloro-N-methylpiperidine; N-methyl-4-chloropiperidine 55770-77-4 C6H12ClN 详情 详情
(IV) 20645 chloro(1-methyl-4-piperidinyl)magnesium C6H12ClMgN 详情 详情
(V) 53286 11-hydroxy-11-(1-methyl-4-piperidinyl)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine-8-carbonitrile n/a C21H23N3O 详情 详情
Extended Information