反応式
[Na].[NH:2]1[CH:6]=[N:5][CH:4]=[N:3]1.Cl[CH2:8][C:9]([NH:11][C:12]1[CH:17]=[CH:16][C:15]([C:18]([N:20]2[C:26]3[CH:27]=[CH:28][CH:29]=[CH:30][C:25]=3[CH2:24][N:23]3[CH:31]=[CH:32][CH:33]=[C:22]3[CH2:21]2)=[O:19])=[CH:14][CH:13]=1)=[O:10]>CN1CCCN(C)C1=O>[CH:33]1[CH:32]=[CH:31][N:23]2[CH2:24][C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][C:26]=3[N:20]([C:18]([C:15]3[CH:14]=[CH:13][C:12]([NH:11][C:9](=[O:10])[CH2:8][N:2]4[CH:6]=[N:5][CH:4]=[N:3]4)=[CH:17][CH:16]=3)=[O:19])[CH2:21][C:22]=12参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
To a suspension of 0.20 g of 1,2,4-triazole sodium in 1 ml of 1,3-dimethyl-3,4,5,6-tetrahydro2(1H)-pyrimidinone is added 0.10 g of 2-chloro-N-[4-(5H-pyrrolo[2,1-c][1,4]benzodiazepin-10(11H)-ylcarbonyl)phenyl] acetamide in 1 ml of 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone followed by stirring at room temperature for 3 hours. The reaction mixture is quenched with 15 ml of water and the resulting solid is collected, washed with water and hexanes to give 70 mg of the desired product as a tan solid. MS(CI): 413(M+H).
後処理
- customThe reaction mixture is quenched with 15 ml of water
- customthe resulting solid is collected
- washwashed with water and hexanes
出典と根拠
- ORDレコード
- ord-c6f354e455804c799e12d7631faff7c9
- 出典データセット
- uspto-grants-1996_05
- 特許番号
- US05516774
関連ノート
読み込み中…