반응식
[ClH:1].[N:2]1([CH2:8][CH2:9][CH2:10][O:11][C:12]2[CH:20]=[CH:19][C:15]([C:16](O)=[O:17])=[CH:14][CH:13]=2)[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3]1>S(Cl)(Cl)=O>[ClH:1].[N:2]1([CH2:8][CH2:9][CH2:10][O:11][C:12]2[CH:20]=[CH:19][C:15]([C:16]([Cl:1])=[O:17])=[CH:14][CH:13]=2)[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3]1참가 물질
3
실험 절차
4-(3-Piperidin-1-ylpropoxy)benzoic acid hydrochloride (D2) (0.23 g) in thionyl chloride (5 ml) was heated under reflux for 1 h. The reaction mixture was then evaporated to a minimum and co-evaporated from DCM (3×10 ml) to give the title compound (D3) as a white powder (0.24 g).
후처리
- temperatureunder reflux for 1 h
- customThe reaction mixture was then evaporated to a minimum
출처 및 근거
- ORD 기록
- ord-67c8ebd31205405786cdabfc6fd90b85
- 출처 데이터셋
- uspto-grants-2008_11
- 특허 번호
- US07446103B2
연결된 노트
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