반응식
[N+:1]([C:4]1[CH:10]=[CH:9][C:8]([C:11]([F:14])([F:13])[F:12])=[CH:7][C:5]=1[NH2:6])([O-:3])=[O:2].Br[CH2:16][CH:17]1[CH2:32][CH2:31][CH2:30][C:19]2([O:23][C:22](=[O:24])[N:21]([CH2:25][C:26]([CH3:29])([CH3:28])[CH3:27])[CH2:20]2)[CH2:18]1.C(=O)([O-])[O-].[Cs+].[Cs+].[Cl-].[NH4+]>CN(C=O)C>[CH2:25]([N:21]1[CH2:20][C:19]2([CH2:30][CH2:31][CH2:32][CH:17]([CH2:16][NH:6][C:5]3[CH:7]=[C:8]([C:11]([F:12])([F:13])[F:14])[CH:9]=[CH:10][C:4]=3[N+:1]([O-:3])=[O:2])[CH2:18]2)[O:23][C:22]1=[O:24])[C:26]([CH3:29])([CH3:28])[CH3:27]참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
반응 조건
- 온도
- 60 °C
실험 절차
A solution containing 2-nitro-5-(trifluoromethyl)aniline (0.777 g, 3.77 mmol) and 7-(bromomethyl)-3-neopentyl-1-oxa-3-azaspiro[4.5]decan-2-one (1.00 g, 3.14 mmol) in DMF (15 mL) was treated with cesium carbonate (3.07 g, 9.43 mmol) and stirred at 60° C. overnight. The cooled reaction mixture was diluted with saturated, aqueous ammonium chloride solution, and the product was extracted into DCM. The organics were washed with brine, dried over Na2SO4, and concentrated. The residue was purified on a 120 g silica gel column (10-60 EtOAc/hexanes; 65 mL/min elution; 254 nm detection) to afford the title compound (0.260 g, 19 yield). MS (m/z) 444.2 (M+H+).
후처리
- customThe cooled reaction mixture
- extractionthe product was extracted into DCM
- washThe organics were washed with brine
- dry with materialdried over Na2SO4
- concentrationconcentrated
- customThe residue was purified on a 120 g silica gel column (10-60 EtOAc/hexanes; 65 mL/min elution; 254 nm detection)
출처 및 근거
- ORD 기록
- ord-b430131e6fab47568898c5403af08fa0
- 출처 데이터셋
- uspto-grants-2015_01
- 특허 번호
- US08927585B2
연결된 노트
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