反応式
BrC1C=CC=CC=1S.C(OC(N1CCC(=O)CC1)=O)(C)(C)C.[C:23]([O:27][C:28]([N:30]1[CH2:35][CH2:34][C:33]([C:37]2[CH:42]=[C:41](F)[CH:40]=[CH:39][C:38]=2[SH:44])([OH:36])[CH2:32][CH2:31]1)=[O:29])([CH3:26])([CH3:25])[CH3:24]>>[C:23]([O:27][C:28]([N:30]1[CH2:31][CH2:32][C:33]([OH:36])([C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][C:38]=2[SH:44])[CH2:34][CH2:35]1)=[O:29])([CH3:26])([CH3:24])[CH3:25]参加物
4
実験手順
This intermediate was prepared from 2-bromo-benzenethiol and 4-oxo-piperidine-1-carboxylic acid tert-butyl ester in a similar way as described for 4-(5-fluoro-2-mercapto-phenyl)-4-hydroxy-piperidine-1-carboxylic acid tert-butyl ester.
出典と根拠
- ORDレコード
- ord-b73883d285c14f8994f382c64271343a
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07732463B2
関連ノート
読み込み中…