반응식
Br[CH2:2][CH:3]=[CH:4][CH2:5][O:6][C:7]1[CH:23]=[CH:22][C:10]2[C:11]([C:15]3[CH:20]=[CH:19][C:18]([Br:21])=[CH:17][CH:16]=3)=[N:12][O:13][CH2:14][C:9]=2[CH:8]=1.[CH2:24]([NH:27][CH3:28])[CH:25]=[CH2:26].C(=O)([O-])[O-].[K+].[K+]>CC(C)=O>[CH2:24]([N:27]([CH2:2]/[CH:3]=[CH:4]/[CH2:5][O:6][C:7]1[CH:23]=[CH:22][C:10]2[C:11]([C:15]3[CH:20]=[CH:19][C:18]([Br:21])=[CH:17][CH:16]=3)=[N:12][O:13][CH2:14][C:9]=2[CH:8]=1)[CH3:28])[CH:25]=[CH2:26]참가 물질
5
실험 절차
1.35 g of 7-(4-bromo-but-2-enyloxy)-4-(4-bromo-phenyl)-1H-benzo[d][1,2]oxazine are dissolved in 50 ml of acetone and treated with 3.83 ml of N-allyl-methyl-amine and 1.28 g of potassium carbonate. The mixture is stirred and subsequently filtered. After concentration the filtrate is chromatographed over silica gel with toluene/acetone/triethylamine (92:7:1). There are obtained 1.09 g of (E)-allyl-[4-[4-(4-bromo-phenyl)-1H-benzo[d][1,2]oxazin-7-yloxy]-but-2-enyl]-methyl-amine which is converted into the fumarate, MS: m/e 427 (M+H+, 1 Br).
후처리
- filtrationsubsequently filtered
- concentrationAfter concentration the filtrate
- customis chromatographed over silica gel with toluene/acetone/triethylamine (92:7:1)
출처 및 근거
- ORD 기록
- ord-4a2b3eea236f4807a6b6f8951e092b31
- 출처 데이터셋
- uspto-grants-1999_01
- 특허 번호
- US05856503
연결된 노트
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