Water → 1-hydroxymethyl-9-chloro-7-phenylpyrimido[1,2-a][1,4]benzodiazepin-3(5H)-one
反応式
[C:1]([C:5]1[N:10]2[C:11]3[CH:25]=[CH:24][C:23]([Cl:26])=[CH:22][C:12]=3[C:13]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)=[N:14][CH2:15][C:9]2=[N:8][C:7](=[O:27])[CH:6]=1)(OC)=[O:2].[H-].[Al+3].[Li+].[H-].[H-].[H-].O.[OH-].[Na+]>O1CCCC1>[OH:2][CH2:1][C:5]1[N:10]2[C:11]3[CH:25]=[CH:24][C:23]([Cl:26])=[CH:22][C:12]=3[C:13]([C:16]3[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=3)=[N:14][CH2:15][C:9]2=[N:8][C:7](=[O:27])[CH:6]=1参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
A solution of 1 mmole of 1-carbomethoxy-9-chloro-7-phenylpyrimido[1,2-a][1,4]benzodiazepin-3(5H)-one in tetrahydrofuran was reacted at room temperature with the stoichiometric amount of lithium aluminum hydride and stirred for several hours. It was decomposed with water and 15% sodium hydroxide and worked up to give 1-hydroxymethyl-9-chloro-7-phenylpyrimido[1,2-a][1,4]benzodiazepin-3(5H)-one.
出典と根拠
- ORDレコード
- ord-a39f1c1df67646c28f17abe2667c0276
- 出典データセット
- uspto-grants-1990_12
- 特許番号
- US04978753
反応ノート
読み込み中…