반응 #4141
ord-4793acac75d84b23abda4b52e9f8c0da
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반응물
시약
반응 조건
후처리
- 1workup.ADDITIONwas added
- 2workup.WAITAfter one hour
- 3workup.ADDITIONwas added over 0.5 hour
- 4workup.STIRRINGThe reaction mixture was stirred under nitrogen at room temperature overnight
- 5workup.STIRRINGthe mixture was stirred 0.5 hour
- 6기타The organic phase was separated
- 7세척washed 4 times with water
- 8건조dried over anhydrous sodium sulfate
- 9기타evaporated in a 100° C. bath in vacuo
- 10workup.DISSOLUTIONThe residue was dissolved in toluene (40 ml)
- 11세척eluted with dichloromethane-methanol (98:2)
- 12기타evaporated
실험 절차
1-(4-Bromo-2-aminophenyl)-1,2,3,4-tetrahydroquinoline (10.6 g, 0.035 mole) was dissolved on a steam bath in dichloromethane (150 ml). The solution was cooled to -5° C. in ice/methanol and triethylamine (5.01 g, 0.050 mole) was added in one portion, followed by a solution of phenylchloroformate (7.85 g, 0.050 mole) dissolved in dichloromethane (10 ml), dropwise over 15 minutes. The mixture was stirred 1 hour in the cold, 2 hours at room temperature, and an additional charge of phenylchloroformate (1.57 g, 0.010 mole) was added. After one hour, a solution of N-methylpiperazine (14.1 g, 0.14 mole) dissolved in dichloromethane (15 ml) was added over 0.5 hour. The reaction mixture was stirred under nitrogen at room temperature overnight. Water (100 ml) was added and the mixture was stirred 0.5 hour. The organic phase was separated, washed 4 times with water, dried over anhydrous sodium sulfate, and evaporated in a 100° C. bath in vacuo. The residue was dissolved in toluene (40 ml), adsorbed on a column of silica gel (500 g) packed in toluene and eluted with dichloromethane-methanol (98:2). The appropriate fractions were combined and evaporated to give 9.2 g (61%) of product, as an oil.