Trifluoroacetic acid → 2-[(3R*,4S*)-1-{[2-Chloro-6-(trifluoromethyl)phenyl]methyl}-3-{[1-(cyclohex-1-en-1-ylmethyl)piperidin-4-yl]carbamoyl}-4-methylpyrrolidin-3-yl]acetic acid

HRID 446017ノート

反応式

HRID 446017 の反応式
FC(F)(F)C(O)=O.[Cl:8][C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([C:15]([F:18])([F:17])[F:16])[C:10]=1[CH2:19][N:20]1[CH2:24][C@@H:23]([CH3:25])[C@@:22]([CH2:42][C:43]([O:45]C(C)(C)C)=[O:44])([C:26](=[O:41])[NH:27][CH:28]2[CH2:33][CH2:32][N:31]([CH2:34][C:35]3[CH2:40][CH2:39][CH2:38][CH2:37][CH:36]=3)[CH2:30][CH2:29]2)[CH2:21]1>ClCCl>[Cl:8][C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([C:15]([F:16])([F:18])[F:17])[C:10]=1[CH2:19][N:20]1[CH2:24][C@@H:23]([CH3:25])[C@@:22]([CH2:42][C:43]([OH:45])=[O:44])([C:26](=[O:41])[NH:27][CH:28]2[CH2:33][CH2:32][N:31]([CH2:34][C:35]3[CH2:40][CH2:39][CH2:38][CH2:37][CH:36]=3)[CH2:30][CH2:29]2)[CH2:21]1

参加物

4

実験手順

Trifluoroacetic acid (1.5 ml, 20.3 mmol) was added to a solution of tert-butyl 2-[(3R*,4S*)-1-{[2-chloro-6-(trifluoromethyl)phenyl]methyl}-3-{[1-(cyclohex-1-en-1-ylmethyl)piperidin-4-yl]carbamoyl}-4-methylpyrrolidin-3-yl]acetate obtained in Example 4i (353 mg, 0.577 mmol) in dichloromethane (400 μl), which was stirred at mom temperature for two hours. The reaction mixture was concentrated under reduced pressure and purified by ODS column chromatography (elution solvent: methanol/water) to give the title compound (215 mg, yield 67%).

後処理

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. custompurified by ODS column chromatography (elution solvent: methanol/water)

出典と根拠

ORDレコード
ord-94461e98f0084997baa80e4aff7eee8f
出典データセット
uspto-grants-2013_07
特許番号
US08476301B2

反応ノート

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