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【结 构 式】

【分子编号】67138

【品名】6-bromo-4-phenylchroman-2-one

【CA登记号】156755-23-6

【 分 子 式 】C15H11BrO2

【 分 子 量 】303.155

【元素组成】C 59.43% H 3.66% Br 26.36% O 10.55%

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:(II)

 

1 Charugundla Kishore, Kumar Udhaya, Patil Rajendra Suryabhan. 2009. An improved process for the preparation of fesoterodine. WO 2009037569.
2 Neela Praveen Kumar, Charugundla Kishore, Kumar Udhaya, et al. 2010. Fesoterodine substance of dehydroxy impurity. WO 2010010464.
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) 25313 4-bromophenol 106-41-2 C6H5BrO 详情 详情
(II) 67138 6-bromo-4-phenylchroman-2-one 156755-23-6 C15H11BrO2 详情 详情
(III) 67139 methyl 3-(2-(benzyloxy)-5-bromophenyl)-3-phenylpropanoate   C23H21BrO3 详情 详情
(IV) 67140 3-(2-(benzyloxy)-5-bromophenyl)-3-phenylpropan-1-ol   C22H21BrO2 详情 详情
(V) 67141 3-(2-(benzyloxy)-5-bromophenyl)-3-phenylpropyl 4-methylbenzenesulfonate   C29H27BrO4S 详情 详情
(VI) 67142 3-(2-(benzyloxy)-5-bromophenyl)-N,N-diisopropyl-3-phenylpropan-1-amine   C28H34BrNO 详情 详情
(VII) 67143 (2S,3S)-2,3-bis((4-methylbenzoyl)oxy)succinic acid   C20H18O8 详情 详情
(VIII) 67144 (S)-3-(2-(benzyloxy)-5-bromophenyl)-N,N-diisopropyl-3-phenylpropan-1-amine (2S,3S)-2,3-bis((4-methylbenzoyl)oxy)succinate    C28H34BrNO.C20H18O8 详情 详情
(IX) 67145 (S)-3-(2-(benzyloxy)-5-bromophenyl)-N,N-diisopropyl-3-phenylpropan-1-amine   C28H34BrNO 详情 详情
(X) 60854 4-(benzyloxy)-3-[(1R)-3-(diisopropylamino)-1-phenylpropyl]benzoic acid C29H35NO3 详情 详情
(XI) 60855 methyl 4-(benzyloxy)-3-[(1R)-3-(diisopropylamino)-1-phenylpropyl]benzoate C30H37NO3 详情 详情
(XII) 60856 {4-(benzyloxy)-3-[(1R)-3-(diisopropylamino)-1-phenylpropyl]phenyl}methanol C29H37NO2 详情 详情
(XIII) 60858 2-[(1R)-3-(diisopropylamino)-1-phenylpropyl]-4-(hydroxymethyl)phenol C22H31NO2 详情 详情
(XV) 67137 cinnamic acid 140-10-3 C9H8O2 详情 详情
Extended Information