반응식
CS(O)(=O)=O.O[CH2:7][CH2:8][CH2:9][N:10]1[C:14]2[CH:15]=[CH:16][C:17]([CH3:19])=[CH:18][C:13]=2[NH:12][C:11]1=[O:20].[C:21]1([N:27]2[C:31]3([CH2:36][CH2:35][NH:34][CH2:33][CH2:32]3)[C:30](=[O:37])[NH:29][CH2:28]2)[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1.C(=O)([O-])[O-].[Na+].[Na+]>CN(C)C=O>[CH3:19][C:17]1[CH:16]=[CH:15][C:14]2[N:10]([CH2:9][CH2:8][CH2:7][N:34]3[CH2:33][CH2:32][C:31]4([N:27]([C:21]5[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=5)[CH2:28][NH:29][C:30]4=[O:37])[CH2:36][CH2:35]3)[C:11](=[O:20])[NH:12][C:13]=2[CH:18]=1참가 물질
반응물 3
생성물 1
시약·촉매·용매 1
반응 조건
- 온도
- 60 °C
실험 절차
A mixture of 5.68 parts of 1,3-dihydro-1-(3-hydroxypropyl)-5-methyl-2H-benzimidazol-2-one methanesulfonate, 4.62 parts of 1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one, 3.7 parts of sodium carbonate and 45 parts of N,N-dimethylformamide is stirred for 1 hour at 60° C. The reaction mixture is cooled and poured onto water. The precipitated product is filtered off and purified by column-chromatography over silica gel using a mixture of trichloromethane and 10% of methanol as eluent. The pure fractions are collected and the eluent is evaporated. The residue is crystallized from a mixture of N,N-dimethylformamide and water, yielding 2 parts (24%) of 8-[3-(1,3-dihydro-5-methyl-2-oxo-2H-benzimidazol-1-yl)propyl]-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one; mp. 255.5° C.
후처리
- temperatureThe reaction mixture is cooled
- additionpoured onto water
- filtrationThe precipitated product is filtered off
- custompurified by column-chromatography over silica gel using
- additiona mixture of trichloromethane and 10% of methanol as eluent
- customThe pure fractions are collected
- customthe eluent is evaporated
- customThe residue is crystallized from a mixture of N,N-dimethylformamide and water
출처 및 근거
- ORD 기록
- ord-e0a9860d9ec8465a988c31ecbd382387
- 출처 데이터셋
- uspto-grants-1979_11
- 특허 번호
- US04175129
연결된 노트
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