반응식
[F:1][C:2]([F:16])([F:15])[C:3]1[CH:4]=[CH:5][C:6]([N:9]2[CH2:14][CH2:13][NH:12][CH2:11][CH2:10]2)=[N:7][CH:8]=1.[Cl:17][C:18]1[CH:19]=[CH:20][C:21]2[N:22]([CH:24]=[C:25]([CH2:27]Cl)[N:26]=2)[CH:23]=1.C(N(CC)CC)C>C(O)CO>[Cl:17][C:18]1[CH:19]=[CH:20][C:21]2[N:22]([CH:24]=[C:25]([CH2:27][N:12]3[CH2:11][CH2:10][N:9]([C:6]4[CH:5]=[CH:4][C:3]([C:2]([F:1])([F:15])[F:16])=[CH:8][N:7]=4)[CH2:14][CH2:13]3)[N:26]=2)[CH:23]=1참가 물질
실험 절차
A mixture of 1-(5-trifluoromethylpyridin-2-yl)piperazine (0.4803 g), 6-chloro-2-(chloromethyl) imidazo[1,2-a]pyridine (Example 4, Step 1; 0.4177 g), triethylamine (0.231 g), and ethylene glycol (1 mL) is stirred at 80° C. for 70 min. after which additional 6-chloro-2-(chloromethyl)imidazo[1,2-a]pyridine (0.072 g) is added; thirty minutes later another portion (0.0517 g) is added. After stirring for a total of 2 h, the mixture is cooled and partitioned between dichloromethane and aq. sodium bicarbonate. The organic layers are dried over sodium sulfate and concentrated. Chromatography on silica gel using methanol/dichloromethane (4/96) and crystallization from ethyl ether/hexane gives 0.549 g of the title compound; mp 81-82° C.; MS m/z 395; IR (mineral oil) 1617, 1332, 1328, 1112, 1082 cm-1. 1H NMR (CDCl3) δ2.68, 3.69, 3.77, 6.62, 7.14, 7.52, 7.55, 7.61, 8.14, 8.38.
후처리
- additionis added
- additionthirty minutes later another portion (0.0517 g) is added
- temperaturethe mixture is cooled
- custompartitioned between dichloromethane and aq. sodium bicarbonate
- dry with materialThe organic layers are dried over sodium sulfate
- concentrationconcentrated
- custommethanol/dichloromethane (4/96) and crystallization from ethyl ether/hexane
출처 및 근거
- ORD 기록
- ord-771c779c217e4f72a3f32110133b22b5
- 출처 데이터셋
- uspto-grants-1999_06
- 특허 번호
- US05912246
연결된 노트
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