반응식
[CH2:1]([O:3][C:4]([C:6]1[CH:10]=[C:9]([C:11]([O:13][CH2:14]C)=[O:12])[NH:8][N:7]=1)=[O:5])C.[H-].[Na+].Br[CH2:19][C:20]1[CH:24]=[C:23]([C:25]2[S:26][C:27]([Cl:30])=[CH:28][CH:29]=2)[O:22][N:21]=1.O>CN(C=O)C>[CH3:14][O:13][C:11]([C:9]1[CH:10]=[C:6]([C:4]([O:3][CH3:1])=[O:5])[N:7]([CH2:19][C:20]2[CH:24]=[C:23]([C:25]3[S:26][C:27]([Cl:30])=[CH:28][CH:29]=3)[O:22][N:21]=2)[N:8]=1)=[O:12]참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
To a solution of 1 g 1H-Pyrazole-3,5-dicarboxylic acid diethyl ester in 20 ml of DMF and 188 mg of sodium hydride (60% in mineral oil) were added at RT. After stirring for 20 min at room temperature 1.32 g of 3-bromomethyl-5-(5-chloro-thiophen-2-yl)-isoxazole were added. The reaction was stirred at room temperature for 3 h. Then 100 ml water were added and the precipitating product was collected by filtration. Yield: 1.7 g.
후처리
- additionwere added
- filtrationthe precipitating product was collected by filtration
출처 및 근거
- ORD 기록
- ord-ac6f8b5ce4bf4aab908a7d48d79f7d5c
- 출처 데이터셋
- uspto-grants-2008_09
- 특허 번호
- US07429581B2
연결된 노트
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