Diethyl Ether → HCID 12763984, 화합물
반응식
[NH2:1][C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][C:8]=2[Cl:12])[N:3]=1.Br[CH2:14][C:15](=O)[C:16]([O:18][CH2:19][CH3:20])=[O:17].C1OC1C.CCOCC>C(COC)OC>[Cl:12][C:8]1[CH:7]=[CH:6][CH:5]=[C:4]2[C:9]=1[CH:10]=[CH:11][C:2]1[N:3]2[CH:14]=[C:15]([C:16]([O:18][CH2:19][CH3:20])=[O:17])[N:1]=1참가 물질
실험 절차
140 mg of 2-amino-5-chloroquinoline were dissolved in 2.5 ml of dimethoxyethane and then a mixture of 170 mg of ethyl bromopyruvate and 30 mg of propylene oxide was added. The mixture was stirred at room temperature for 2 hours and 2 ml of ether were added. Then, the mixture was cooled in ice and the precipitated quaternary salt was filtered off, was dissolved in 5 ml of ethanol and the solution was heated at reflux for 2 hours. Then, the solvent was removed under vacuum and the residue was partitioned between sodium bicarbonate solution and chloroform. The chloroform solution was dried over magnesium sulfate and was evaporated to dryness. The residue was chromatographed over silica with chloroform as eluent and the purified product was recrystallized from ethyl acetate/petroleum ether to obtain colorless needles of ethyl 6-chloroimidazo-[1,2-a]-quinoline-2-carboxylate melting at 193°-194° C.
후처리
- additionwas added
- temperatureThen, the mixture was cooled in ice
- filtrationthe precipitated quaternary salt was filtered off
- dissolutionwas dissolved in 5 ml of ethanol
- temperaturethe solution was heated
- temperatureat reflux for 2 hours
- customThen, the solvent was removed under vacuum
- customthe residue was partitioned between sodium bicarbonate solution and chloroform
- dry with materialThe chloroform solution was dried over magnesium sulfate
- customwas evaporated to dryness
- customThe residue was chromatographed over silica with chloroform as eluent
- customthe purified product was recrystallized from ethyl acetate/petroleum ether
출처 및 근거
- ORD 기록
- ord-3e35b2e4683447e7b6fdd667d5564f13
- 출처 데이터셋
- uspto-grants-1981_07
- 특허 번호
- US04279912
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