反応式
[CH:1]([N:4]([CH2:8][CH2:9][NH2:10])[CH:5]([CH3:7])[CH3:6])([CH3:3])[CH3:2].[C:11](N1C=CN=C1)(N1C=CN=C1)=[O:12].[C:23]1([S:29]([CH:32]2[CH2:37][CH2:36][CH2:35][NH:34][CH2:33]2)(=[O:31])=[O:30])[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1>>[CH3:2][CH:1]([N:4]([CH:5]([CH3:7])[CH3:6])[CH2:8][CH2:9][NH:10][C:11]([N:34]1[CH2:35][CH2:36][CH2:37][CH:32]([S:29]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)(=[O:31])=[O:30])[CH2:33]1)=[O:12])[CH3:3]参加物
4
実験手順
Following the procedure of Example 16, diisopropylaminoethylamine and 1,1'-carbonyldiimidazole and 3-(phenylsulfonyl)piperidine were reacted to give the title compound which was crystallized from diethyl ether-hexane as white solid in 59.8% yield, m.p. 82.5°-84° C.
後処理
- customwere reacted
出典と根拠
- ORDレコード
- ord-c6a1da51d6b645619f3932338d5acfbd
- 出典データセット
- uspto-grants-1987_02
- 特許番号
- US04642348
関連ノート
読み込み中…