반응식
Cl[C:2]1[CH:7]=[C:6]([NH2:8])[CH:5]=[CH:4][N:3]=1.[NH:9]1[CH2:13][CH2:12][CH2:11][CH2:10]1>>[N:9]1([C:2]2[CH:7]=[C:6]([NH2:8])[CH:5]=[CH:4][N:3]=2)[CH2:13][CH2:12][CH2:11][CH2:10]1참가 물질
3
반응 조건
- 온도
- 200 °C
실험 절차
A mixture of 2-chloro-4-aminopyridine (2.29 g, 17.8 mmol) and pyrrolidine (5.0 mL) was microwave heated at 200° C. for 10 min. After cooling to room temperature, the solid was filtered and washed with dichloromethane (10 mL×3). The filter cake was dissolved in aqueous K2CO3 and extracted with CH2Cl2 (40 mL×3). The combined organic layers were dried over Na2SO4 and concentrated to obtain 2-(pyrrolidin-1-yl)pyridin-4-amine (2.3 g, 79% yield).
후처리
- temperatureAfter cooling to room temperature
- filtrationthe solid was filtered
- washwashed with dichloromethane (10 mL×3)
- dissolutionThe filter cake was dissolved in aqueous K2CO3
- extractionextracted with CH2Cl2 (40 mL×3)
- dry with materialThe combined organic layers were dried over Na2SO4
- concentrationconcentrated
출처 및 근거
- ORD 기록
- ord-473bbfc4134d46f7b6013c271becb353
- 출처 데이터셋
- uspto-grants-2014_04
- 특허 번호
- US08685970B2
연결된 노트
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