Thiophenol → HCID 66918764、化合物
反応式
[CH2:1]([O:3][C:4]([C@@H:6]1[CH2:10][CH:9](OS(C)(=O)=O)[CH2:8][C@H:7]1[C:16](=[O:23])[NH:17][C:18]1([C:21]#[N:22])[CH2:20][CH2:19]1)=[O:5])[CH3:2].[C:24]1([SH:30])[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1>>[CH2:1]([O:3][C:4]([C@@H:6]1[CH2:10][C@H:9]([S:30][C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)[CH2:8][C@H:7]1[C:16](=[O:23])[NH:17][C:18]1([C:21]#[N:22])[CH2:19][CH2:20]1)=[O:5])[CH3:2]参加物
3
実験手順
The reaction of the mixture of (1R,2R,4R) and (1R,2R,4S)-2-(1-cyano-cyclopropylcarbamoyl)-4-methanesulfonyloxy-cyclopentanecarboxylic acid ethyl ester from step 3 with thiophenol performed in analogy to example 1, step 5, yielded a crude material which was purified on silica using n-heptane/EtOAc (3:2) to give in the first fraction the desired (1R,2R,4R)-2-(1-cyano-cyclopropylcarbamoyl)-4-phenylsulfanyl-cyclopentanecarboxylic acid ethyl ester as a colorless oil. MS: 359.2 (M+H)+.
後処理
- customyielded a crude material which
- customwas purified on silica
出典と根拠
- ORDレコード
- ord-9553e535394a4ee5a0814596846f75d1