反応式
COCCN(S(F)(F)F)CCOC.[C:14]([N:17]1[CH2:21][CH2:20][CH:19](O)[CH:18]1[C:23]1[C:24]([O:38][C:39]2[CH:44]=[CH:43][C:42]([S:45]([CH3:48])(=[O:47])=[O:46])=[CH:41][CH:40]=2)=[CH:25][C:26]2[N:30]=[C:29]([C:31]3[CH:36]=[CH:35][CH:34]=[CH:33][N:32]=3)[NH:28][C:27]=2[CH:37]=1)(=[O:16])[CH3:15]>C(Cl)(Cl)Cl>[C:14]([N:17]1[CH2:21][CH2:20][CH:19]=[C:18]1[C:23]1[C:24]([O:38][C:39]2[CH:40]=[CH:41][C:42]([S:45]([CH3:48])(=[O:46])=[O:47])=[CH:43][CH:44]=2)=[CH:25][C:26]2[N:30]=[C:29]([C:31]3[CH:36]=[CH:35][CH:34]=[CH:33][N:32]=3)[NH:28][C:27]=2[CH:37]=1)(=[O:16])[CH3:15]参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
2 mg of bis(2-methoxyethyl)aminosulfur trifluoride was added to a chloroform (1 ml) solution of 2 mg of 1-acetyl-2-(5-(4-(methanesulfonyl)phenoxy)-2-pyridin-2-yl-1H-benzimidazol-6-yl)pyrrolidin-3-ol diastereomer A obtained in Example 469, and the reaction liquid was stirred at room temperature for 15 minutes. The solvent was evaporated away under reduced pressure, and the resulting residue was purified through partitioning thin-layer chromatography (Kieselgel™ 60F254, Art 5744 (by Merck), chloroform/methanol=15/1) to obtain the entitled compound as a colorless oily substance.
後処理
- customA obtained in Example 469
- customthe reaction liquid
- customThe solvent was evaporated away under reduced pressure
- customthe resulting residue was purified
- customthrough partitioning thin-layer chromatography (Kieselgel™ 60F254, Art 5744 (by Merck), chloroform/methanol=15/1)
- customto obtain the entitled compound as a colorless oily substance
出典と根拠
- ORDレコード
- ord-7826d805fa88468484e7350b593a91a7
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07728025B2
関連ノート
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