Pyridine → [5-(1-Fluoromethyl-cyclopropyl)-2-p-tolyl-2H-pyrazol-3-yl]-carbamic acid 2,2,2-trichloro-ethyl ester
반응식
Cl[C:2]([O:4][CH2:5][C:6]([Cl:9])([Cl:8])[Cl:7])=[O:3].[F:10][CH2:11][C:12]1([C:15]2[CH:16]=[C:17]([NH2:27])[N:18]([C:20]3[CH:25]=[CH:24][C:23]([CH3:26])=[CH:22][CH:21]=3)[N:19]=2)[CH2:14][CH2:13]1.N1C=CC=CC=1.CCOC(C)=O>C1COCC1>[Cl:7][C:6]([Cl:9])([Cl:8])[CH2:5][O:4][C:2](=[O:3])[NH:27][C:17]1[N:18]([C:20]2[CH:21]=[CH:22][C:23]([CH3:26])=[CH:24][CH:25]=2)[N:19]=[C:15]([C:12]2([CH2:11][F:10])[CH2:13][CH2:14]2)[CH:16]=1참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
Slowly add ClCO2CH2CCl3 (1.00 equiv; 717.49 μmoles; 152.01 mg) to a solution of 5-(1-fluoromethyl-cyclopropyl)-2-p-tolyl-2H-pyrazol-3-ylamine (176 mg, 0.71 mmoles) and pyridine in 4 mL of THF under nitrogen at 0° C. Stir the mixture from 0° C. to room temperature for 5 hours. Filter the insoluble and remove solvent from filtrate under reduced pressure give an oil. Subject oil to chromatorgraphy (hex/AcOEt 20-80%) to give 110 mg of title compound as a yellow oil. MS (ES+): m/z=420.0 [M+H].
후처리
- customat 0° C
- filtrationFilter the insoluble and
- customremove solvent from filtrate under reduced pressure
- customgive an oil
출처 및 근거
- ORD 기록
- ord-b045f703638345acbc03b9864b96e4fe
- 출처 데이터셋
- uspto-grants-2010_01
- 특허 번호
- US07652015B2
반응 노트
불러오는 중…