Diisopropyl Ether → 4-Aminomethyl-1-(pyridin-4-yl)piperidine-4-carboxylic acid ethyl ester dihydrobromide
반응식
[CH2:1]([O:3][C:4]([C:6]1([CH2:18][NH:19]C(OCC2C=CC=CC=2)=O)[CH2:11][CH2:10][N:9]([C:12]2[CH:17]=[CH:16][N:15]=[CH:14][CH:13]=2)[CH2:8][CH2:7]1)=[O:5])[CH3:2].[BrH:30].C(O)(=O)C.CCCCCC.C(OC(C)C)(C)C>C(Cl)(Cl)Cl.C(OCC)C>[BrH:30].[BrH:30].[CH2:1]([O:3][C:4]([C:6]1([CH2:18][NH2:19])[CH2:11][CH2:10][N:9]([C:12]2[CH:17]=[CH:16][N:15]=[CH:14][CH:13]=2)[CH2:8][CH2:7]1)=[O:5])[CH3:2]참가 물질
7
반응물 4
생성물 1
시약·촉매·용매 2
실험 절차
To a solution of 4-benzyloxycarbonylaminomethyl-1-(pyridin-4-yl)piperidine-4-carboxylic acid ethyl ester (331 mg) in chloroform (0.5 ml) was added 25% hydrogen bromide-acetic acid (2 ml), and the mixture was stirred at room temperature for 10 min. After completion of the reaction, hexane, diisopropyl ether and diethyl ether were added and the supernatant was removed. Then, dimethylformamide (1 ml) was added and the resultant solid was collected by filtration, and washed with diethyl ether and dried under reduced pressure to give the title compound (423 mg).
후처리
- additionwere added
- customthe supernatant was removed
- additionThen, dimethylformamide (1 ml) was added
- filtrationthe resultant solid was collected by filtration
- washwashed with diethyl ether
- customdried under reduced pressure
출처 및 근거
- ORD 기록
- ord-638c12e62b5b49f0942c0610889731d2
- 출처 데이터셋
- uspto-grants-2003_05
- 특허 번호
- US06562828B1
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