Tert-butyl {3-[5-(2,4-dioxothiazolidin-5-ylidenemethyl)thiophen-2-yl]benzyl}methylcarbamate → Tert-butyl {3-[5-(2,4-dioxothiazolidin-5-ylmethyl)thiophen-2-yl]benzyl}methylcarbamate
反応式
[O:1]=[C:2]1[NH:6][C:5](=[O:7])[C:4](=[CH:8][C:9]2[S:13][C:12]([C:14]3[CH:15]=[C:16]([CH:27]=[CH:28][CH:29]=3)[CH2:17][CH2:18][NH:19][C:20](=[O:26])[O:21][C:22]([CH3:25])([CH3:24])[CH3:23])=[CH:11][CH:10]=2)[S:3]1>O1CCOCC1.C(O)(=O)C>[O:1]=[C:2]1[NH:6][C:5](=[O:7])[CH:4]([CH2:8][C:9]2[S:13][C:12]([C:14]3[CH:15]=[C:16]([CH:27]=[CH:28][CH:29]=3)[CH2:17][CH2:18][NH:19][C:20](=[O:26])[O:21][C:22]([CH3:25])([CH3:23])[CH3:24])=[CH:11][CH:10]=2)[S:3]1参加物
4
実験手順
1 g (2.5 mmol) of tert-butyl {3-[5-(2,4-dioxothiazolidin-5-ylidenemethyl)thiophen-2-yl]benzyl}methylcarbamate is placed in 20 ml of dioxane and 0.2 ml of acetic acid. The reaction medium is degassed and placed under 3 atm of hydrogen for 3 days. After filtration through Celite, 0.2 g (20%) of tert-butyl {3-[5-(2,4-dioxothiazolidin-5-ylmethyl)thiophen-2-yl]benzyl}methylcarbamate is obtained.
後処理
- customThe reaction medium is degassed
- filtrationAfter filtration through Celite
出典と根拠
- ORDレコード
- ord-7f66d4f0eeb347039b80b8586c4cef56
- 出典データセット
- uspto-grants-2011_09
- 特許番号
- US08022079B2
反応ノート
読み込み中…