Hydrochloric Acid → HCID 21584328, 화합물
반응식
[N+:1]([C:4]1[CH:18]=[CH:17][C:7]2[CH2:8][CH:9]3[N:14]([C:15](=O)[C:6]=2[CH:5]=1)[CH2:13][CH2:12][CH2:11][CH2:10]3)([O-:3])=[O:2].B.[ClH:20]>C1COCC1.C(O)C>[ClH:20].[N+:1]([C:4]1[CH:18]=[CH:17][C:7]2[CH2:8][CH:9]3[N:14]([CH2:15][C:6]=2[CH:5]=1)[CH2:13][CH2:12][CH2:11][CH2:10]3)([O-:3])=[O:2]참가 물질
실험 절차
To a solution of 8-nitro-1,3,4,6,11,11a-hexahydro-2H-benzo[b]quinolizin-6-one (4.18 g, 17.0 mmol) in anhydrous THF (50 ml) was added 1.0M borane in THF (50 ml). The reaction mixture was heated at reflux for 18 h. After cooling to room temperature, the excess borane was quenched by the addition of methanol and 6M hydrochloric acid (6 ml) and the solution was heated for 2 h. The solvent was removed in vacuo and the residue was taken up in water. The resulting solution was basified with sodium hydroxide and extracted twice with dichloromethane. The dried (magnesium sulfate) organic phase was concentrated to give an oil which was immediately taken up in ethanol (60 ml). Hydrochloric acid in ethanol was added until the solution was distinctly acidic and the solution was stirred for several hours at ambient temperature. The precipitate was collected, washed with ethanol, and air-dried to give the title compound as a white solid (3.03 g, 70%), m.p. 245-7° C. (dec.).
후처리
- temperatureThe reaction mixture was heated
- temperatureat reflux for 18 h
- customthe excess borane was quenched by the addition of methanol and 6M hydrochloric acid (6 ml)
- temperaturethe solution was heated for 2 h
- customThe solvent was removed in vacuo
- extractionextracted twice with dichloromethane
- dry with materialThe dried (magnesium sulfate) organic phase
- concentrationwas concentrated
- customto give an oil which
- customThe precipitate was collected
- washwashed with ethanol
- customair-dried
출처 및 근거
- ORD 기록
- ord-e15bece9873640148144c9c7a316b83a
- 출처 데이터셋
- uspto-grants-1999_07
- 특허 번호
- US05929085
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