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【结 构 式】

【分子编号】35051

【品名】methyl (1S,2R,3S,5R)-3-(4-chloro-3-methylphenyl)-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylate

【CA登记号】

【 分 子 式 】C17H22ClNO2

【 分 子 量 】307.81992

【元素组成】C 66.33% H 7.2% Cl 11.52% N 4.55% O 10.4%

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:(IIIb)

Conjugate addition of 4-chloro-3-methylphenylmagnesium iodide (II) to anhydroecgonine methyl ester (I) at -40 C, followed by quenching with trifluoroacetic acid at -78 C afforded a 1:1.6 mixture of 2alpha and 2beta-3-aryltropane-2-carboxylate esters (III). The target 2beta-isomer was then isolated by column chromatography.

1 Suslu, I.; Altinoz, S.; Med Chem Res 1992, 1, 6, 382-387.
2 Carroll, F.I.; Mascarella, S.W.; Kuzemko, M.A.; Gao, Y.; Abraham, P.; Lewin, A.H.; Boja, J.W.; Kuhar, M.J.; Synthesis, ligand binding, and QSAR (CoMFA and classical) study of 3beta-(3'-substituted phenyl)-, 3beta-(4'-substituted phenyl)-, and 3beta-(3', 4'-disubstituted phenyl)tropane-2beta-carboxylic acid methyl esters. J Med Chem 1994, 37, 18, 2865.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(IIIa) 35050 methyl (1S,2S,3S,5R)-3-(4-chloro-3-methylphenyl)-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylate C17H22ClNO2 详情 详情
(IIIb) 35051 methyl (1S,2R,3S,5R)-3-(4-chloro-3-methylphenyl)-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylate C17H22ClNO2 详情 详情
(I) 21118 methyl (1R,5S)-8-methyl-8-azabicyclo[3.2.1]oct-2-ene-2-carboxylate C10H15NO2 详情 详情
(II) 35049 (4-chloro-3-methylphenyl)(iodo)magnesium C7H6ClIMg 详情 详情
Extended Information