反応式
Cl.[CH3:2][NH2:3].[CH3:4][C:5]([O:8][C:9]([NH:11][CH:12]([C:19]([OH:21])=O)[CH2:13][C:14]1[N:18]=[CH:17][S:16][CH:15]=1)=[O:10])([CH3:7])[CH3:6]>>[C:5]([O:8][C:9]([NH:11][C@@H:12]([CH2:13][C:14]1[N:18]=[CH:17][S:16][CH:15]=1)[C:19]([NH:3][CH3:2])=[O:21])=[O:10])([CH3:4])([CH3:6])[CH3:7]参加物
3
実験手順
Methylamine hydrochloride (1.2 mmol) and Boc-L-3-(4-thiazolyl)alanine (1.0 mmol) were coupled according to Procedure A (0-25° C. reaction temperature, acid wash omitted) and the product used without further purification. Yield, 250 mg, 88%.
後処理
- customthe product used without further purification
- customYield
出典と根拠
- ORDレコード
- ord-90522270a7bc4643827350fc855ef981
- 出典データセット
- uspto-grants-2000_08
- 特許番号
- US06107329
関連ノート
読み込み中…