반응식
Cl[CH:2]([C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)[C:3]([NH:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]([N:14]2[C:20]3[CH:21]=[CH:22][CH:23]=[CH:24][C:19]=3[CH2:18][N:17]3[CH:25]=[CH:26][CH:27]=[C:16]3[CH2:15]2)=[O:13])=[CH:8][CH:7]=1)=[O:4].[CH3:34][NH:35][CH3:36].CN1CCCN(C)C1=O.C(OCC)(=O)C.CCCCCC>CO>[CH3:34][N:35]([CH3:36])[CH:2]([C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)[C:3]([NH:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]([N:14]2[C:20]3[CH:21]=[CH:22][CH:23]=[CH:24][C:19]=3[CH2:18][N:17]3[CH:25]=[CH:26][CH:27]=[C:16]3[CH2:15]2)=[O:13])=[CH:8][CH:7]=1)=[O:4]참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
A partial solution of ??g of α-chloro-N-[4-(5H-pyrrolo[2,1-c][1,4]benzodiazepin-10(11H)-ylcarbonyl)phenyl]benzeneacetamide in 1 ml of methanol is treated with 0.5 ml of dimethylamine and 1 ml of 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone and stirring continued for 20 hours. The methanol is evaporated and the residue diluted with water. The resulting solid is washed with water, dissolved in ethyl acetate and the organic layer washed with saturated NaHCO3, brine and dried with Na2SO4. The mixture is filtered and the filtrate evaporated vacuo to give a residue which is stirred with ethyl acetate-hexane to give 0.15 g of a beige solid. MS(CI): 465(M+H).
후처리
- customThe methanol is evaporated
- additionthe residue diluted with water
- washThe resulting solid is washed with water
- dissolutiondissolved in ethyl acetate
- washthe organic layer washed with saturated NaHCO3, brine
- dry with materialdried with Na2SO4
- filtrationThe mixture is filtered
- customthe filtrate evaporated vacuo
- customto give a residue which
출처 및 근거
- ORD 기록
- ord-718639caf7174c93bb881dc3f18a8de8
- 출처 데이터셋
- uspto-grants-1996_05
- 특허 번호
- US05516774
연결된 노트
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