Hydrochloric Acid → 2-Phenyl-5-(pyrrolidin-1-ylmethyl)thiazole-4-carboxylate hydrochloride
反応式
[ClH:1].[C:2]1([C:8]2[S:9][C:10]([CH2:20][N:21]3[CH2:25][CH2:24][CH2:23][CH2:22]3)=[C:11]([C:13]([O:15]C(C)(C)C)=[O:14])[N:12]=2)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>C1COCC1>[ClH:1].[C:2]1([C:8]2[S:9][C:10]([CH2:20][N:21]3[CH2:25][CH2:24][CH2:23][CH2:22]3)=[C:11]([C:13]([OH:15])=[O:14])[N:12]=2)[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1参加物
4
実験手順
Concentrated HCl (2.8 ml, 33.9 mmol) was added to a solution of tert-butyl 2-phenyl-5-(pyrrolidin-1-ylmethyl)thiazole-4-carboxylate (2.1 g, 6.1 mmol) in THF (30 ml). The mixture was stirred at rt overnight, and concentrated in vacuo to give 2-phenyl-5-(pyrrolidin-1-ylmethyl)thiazole-4-carboxylate hydrochloride (1.5 g, 82% yield).
後処理
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-dd6ed0a6c7d747779ad1d21e8251e6cb
- 出典データセット
- uspto-grants-2013_07
- 特許番号
- US08492401B2
反応ノート
読み込み中…