반응식
C([N:8]1[CH2:13][CH2:12][N:11]([C:14]2[CH:15]=[CH:16][CH:17]=[C:18]3[C:23]=2[N:22]=[CH:21][CH:20]=[CH:19]3)[CH2:10][CH2:9]1)C1C=CC=CC=1.ClC(OC=C)=O>C(Cl)Cl>[N:11]1([C:14]2[CH:15]=[CH:16][CH:17]=[C:18]3[C:23]=2[N:22]=[CH:21][CH:20]=[CH:19]3)[CH2:12][CH2:13][NH:8][CH2:9][CH2:10]1참가 물질
실험 절차
To a solution of 8-(4-benzyl-piperazin-1-yl)quinoline (2.63 g, 8.7 mmol) in methylene chloride (30 ml) was added vinyl chloroformate (1.1 ml, 13 mmol) at room temperature slowly. The reaction mixture was refluxed for 2 hours, and then concentrated under vacuum. The residue was dissolved in 12 N hydrochloric acid (20 ml) and stirred at room temperature for 1 hour. The mixture was concentrated, the residue was taken up with 40 ml ethanol and heated up to 50° C. for 2 hours. The solvent was removed under vacuum, the residue was dissolved in 1 N sodium hydroxide-ethyl acetate and extracted with ethyl acetate and washed with water. The organic layer was dried over anhydrous sodium sulfate. The solvent was removed under vacuum. Chromatography (10-30% methanol -methylene chloride plus ammonium hydroxide) afforded 1.86 g (90%) yellow oil; MS EI m/e 213 (M)+.
후처리
- temperatureThe reaction mixture was refluxed for 2 hours
- concentrationconcentrated under vacuum
- dissolutionThe residue was dissolved in 12 N hydrochloric acid (20 ml)
- concentrationThe mixture was concentrated
- temperatureheated up to 50° C. for 2 hours
- customThe solvent was removed under vacuum
- dissolutionthe residue was dissolved in 1 N sodium hydroxide-ethyl acetate
- extractionextracted with ethyl acetate
- washwashed with water
- dry with materialThe organic layer was dried over anhydrous sodium sulfate
- customThe solvent was removed under vacuum
출처 및 근거
- ORD 기록
- ord-2e55f5d3b9204febb804c6020b17ff15
- 출처 데이터셋
- uspto-grants-2001_11
- 특허 번호
- US06313126B1
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