o-Chlorophenylacetic acid → Acetyl chloride, 2-(2-chlorophenyl)-

15 ml of thionyl chloride was added to 0.44 g of 2-chlorophenylacetic acid. The mixture was stirred at room temperature for 2 hours. The reaction mixture was subjected to distillation to remove the remaining thionyl chloride and then to azeotropy with toluene twice to completely remove the thionyl chloride. The residue was dissolved in 10 ml of dichloromethane. 0.36 ml of triethylamine was added, with ice-cooling, to a dichloromethane solution containing 0.40 g of 5-dimethylamino-1-(4-aminobenzoyl)-2,3,4,5-tetrahydro-1H-benzoazepine. Thereto was dropwise added the above obtained 2-(2-chlorophenyl)acetyl chloride solution. The resulting mixture was stirred at room temperature for 1 hour. The reaction mixture was water-washed twice, then dried over magnesium sulfate and concentrated. The residue was purified by silica gel column chromatography (elutant: chloroform/methanol=200/1) and then recrystallized from methanol-diethyl ether to obtain 0.29 g of 5-dimethylamino-1-{4-[2-(2-chlorophenyl)acetylamino]benzoyl}-2,3,4,5-tetrahydro-1H-benzoazepine.

1. distillationThe reaction mixture was subjected to distillation
2. customto remove the remaining thionyl chloride
3. customto completely remove the thionyl chloride
4. dissolutionThe residue was dissolved in 10 ml of dichloromethane
5. addition0.36 ml of triethylamine was added, with ice-
6. temperaturecooling, to a dichloromethane solution
7. additioncontaining 0.40 g of 5-dimethylamino-1-(4-aminobenzoyl)-2,3,4,5-tetrahydro-1H-benzoazepine
8. additionThereto was dropwise added the

ORD 기록

ord-d0c460ed1540444c85bf2a050d61eee3

출처 데이터셋

uspto-grants-1997_04

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US05622947