Acetic Acid → (R)-ethyl 1-(2-(1-(4-chloro-1H-pyrazol-1-yl)cyclopropyl)-3H-imidazo[4,5-b]pyridin-5-yl)piperidine-3-carboxylate
반응식
C(O)(=O)C.[NH2:5][C:6]1[CH:7]=[CH:8][C:9]([N:13]2[CH2:18][CH2:17][CH2:16][C@@H:15]([C:19]([O:21][CH2:22][CH3:23])=[O:20])[CH2:14]2)=[N:10][C:11]=1[NH2:12].[Cl:24][C:25]1[CH:26]=[N:27][N:28]([C:30]2([C:33](=N)OCC)[CH2:32][CH2:31]2)[CH:29]=1.C(N(CC)CC)C>C(O)C>[Cl:24][C:25]1[CH:26]=[N:27][N:28]([C:30]2([C:33]3[NH:12][C:11]4=[N:10][C:9]([N:13]5[CH2:18][CH2:17][CH2:16][C@@H:15]([C:19]([O:21][CH2:22][CH3:23])=[O:20])[CH2:14]5)=[CH:8][CH:7]=[C:6]4[N:5]=3)[CH2:32][CH2:31]2)[CH:29]=1참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
Acetic acid (4.3 g, 67.2 mmol) was added to a solution of (R)-ethyl 1-(5,6-diaminopyridin-2-yl)piperidine-3-carboxylate (890 mg, 3.36 mmol), ethyl 1-(4-chloro-1H-pyrazol-1-yl)cyclopropanecarbimidate (445 mg, 1.78 mmol) and triethylamine (0.8 mL, 5.92 mmol) in ethanol (25 mL) at room temperature under a nitrogen atmosphere. The mixture was heated at reflux for 16 h, then was concentrated under reduced pressure. The resulting residue was partitioned between ethyl acetate and water. The organics were dried over sodium sulfate and concentrated under reduced pressure. The crude material was purified via column chromatography (100-200 mesh silica gel, 20-60% ethyl acetate in petroleum ether) to afford (R)-ethyl 1-(2-(1-(4-chloro-1H-pyrazol-1-yl)cyclopropyl)-3H-imidazo[4,5-b]pyridin-5-yl)piperidine-3-carboxylate (600 mg). MS (ES+) (M+H) 415.2859.
후처리
- temperatureThe mixture was heated
- temperatureat reflux for 16 h
- concentrationwas concentrated under reduced pressure
- customThe resulting residue was partitioned between ethyl acetate and water
- dry with materialThe organics were dried over sodium sulfate
- concentrationconcentrated under reduced pressure
- customThe crude material was purified via column chromatography (100-200 mesh silica gel, 20-60% ethyl acetate in petroleum ether)
출처 및 근거
- ORD 기록
- ord-ce7a3ac5e0d74da7846d8ae87da8db76
- 출처 데이터셋
- uspto-grants-2016_03
- 특허 번호
- US09296745B2
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