반응식
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([N:10]2[CH2:14][CH2:13][CH:12]([N:15]3[CH:19]=[CH:18][N:17]=[CH:16]3)[CH2:11]2)=[CH:6][CH:5]=1)([O-:3])=[O:2].[Br:20][C:21](Br)([CH3:23])[CH3:22]>C(O)CCCC.CN(C=O)C>[Br-:20].[Br-:20].[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([N:10]2[CH2:14][CH2:13][CH:12]([N+:15]3[CH:19]=[CH:18][N:17]([CH2:22][CH2:21][CH2:23][N+:17]4[CH:18]=[CH:19][N:15]([CH:12]5[CH2:13][CH2:14][N:10]([C:7]6[CH:6]=[CH:5][C:4]([N+:1]([O-:3])=[O:2])=[CH:9][CH:8]=6)[CH2:11]5)[CH:16]=4)[CH:16]=3)[CH2:11]2)=[CH:6][CH:5]=1)([O-:3])=[O:2]참가 물질
4
반응 조건
- 온도
- 115 °C
실험 절차
3.5 g (0.0135 mol) of 1-[1-(4-nitrophenyl)pyrrolidin-3-yl]-1H-imidazole were heated to 100° C. in 12 ml of a pentanol/DMF mixture (50/50). 1 g (0.005 mol) of dibromopropane was added. The reaction medium was heated at 115° C. for 17 hours. The precipitate was filtered off while hot and washed with pentanol and then with ether. After draining by suction and drying the precipitate, 3.4 g of yellow powder (4) were obtained. 33% yield.
후처리
- filtrationThe precipitate was filtered off while hot and
- washwashed with pentanol
- customdrying the precipitate
출처 및 근거
- ORD 기록
- ord-387f92f2044842899763467dfed4b438
- 출처 데이터셋
- uspto-grants-2005_08
- 특허 번호
- US06923835B2
연결된 노트
불러오는 중…