Trifluoroacetic acid → 13-cyclohexyl-3-methoxy-6-(methoxycarbonyl)-7H-indolo[2,1-a][2]benzazepine-10-carboxylic acid

HRID 1408311노트

반응식

HRID 1408311 반응식
[CH3:1][O:2][C:3]([C:5]1[CH2:31][N:10]2[C:11]3[CH:12]=[C:13]([C:24]([O:26]C(C)(C)C)=[O:25])[CH:14]=[CH:15][C:16]=3[C:17]([CH:18]3[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]3)=[C:9]2[C:8]2[CH:32]=[CH:33][C:34]([O:36][CH3:37])=[CH:35][C:7]=2[CH:6]=1)=[O:4].FC(F)(F)C(O)=O>ClCCl>[CH3:1][O:2][C:3]([C:5]1[CH2:31][N:10]2[C:11]3[CH:12]=[C:13]([C:24]([OH:26])=[O:25])[CH:14]=[CH:15][C:16]=3[C:17]([CH:18]3[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]3)=[C:9]2[C:8]2[CH:32]=[CH:33][C:34]([O:36][CH3:37])=[CH:35][C:7]=2[CH:6]=1)=[O:4]

참가 물질

4

실험 절차

13-Cyclohexyl-3-methoxy-7H-benzo[3,4]azepino[1,2-a]indole-6,10-dicarboxylic acid 10-tert-butyl ester 6-methyl ester 1a (1 g, 1 eq) was dissolved in dry dichloromethane under N2, followed by the addition of trifluoroacetic acid (TFA) (8.88 ml, 60 eq). The solution was stirred at RT for 24 h. The solvent was then removed under reduced pressure. The crude product was triturated with diethyl ether. The crystals were filtered off and dried under vacuum overnight to afford the title product 13-Cyclohexyl-3-methoxy-7H-benzo[3,4]azepino[1,2-a]indole-6,10-dicarboxylic acid 6-methyl ester 13a (89%, 0.86 g); LC-MS: Rt. 3.19 min., m/z 446 [M+H]+.

후처리

  1. customThe solvent was then removed under reduced pressure
  2. customThe crude product was triturated with diethyl ether
  3. filtrationThe crystals were filtered off
  4. customdried under vacuum overnight

출처 및 근거

ORD 기록
ord-31b29ca9a3214ddf916b49d91d9c5086
출처 데이터셋
uspto-grants-2014_12
특허 번호
US08921355B2

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