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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3579생성일: 2026년 10월 24일

Triethylamine → N-[4-(Pyrrolo[1,2-a]quinoxalin-5(4H)-ylcarbonyl)phenyl]-2,3-dichlorobenzamide

https://huagongshe.com/ko/reaction/3579

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2,3-Dichlorobenzoyl chlorideHCID 17944—
반응물4,5-Dihydro-5-(4-aminobenzoyl)pyrrolo[1,2-a]quinoxalineHCID 21837005—
용매DichloromethaneHCID 6344—
생성물N-[4-(Pyrrolo[1,2-a]quinoxalin-5(4H)-ylcarbonyl)phenyl]-2,3-dichlorobenzamideHCID 2183710813.3%

반응 단계

As described for Example 157, 0.47 g of 4,5-dihydro-5-(4-aminobenzoyl)pyrrolo[1,2-a]quinoxaline, 346 μl of triethylamine and 5 ml of dichloromethane are chilled (ice bath) and 0.415 g of 2,3-dichlorobenzoyl chloride in 2 ml of dichloromethane added. After stirring overnight, an additional 346 μl of triethylamine is added and an additional 0.415 g of 2,3-dichlorobenzoyl chloride added. The mixture is stirred for 2 hours, diluted with 50 ml of dichloromethane and the solution washed with 20 ml each of H2O, 2N citric acid, 1M NaHCO3 and brine. The organic layer is dried (Na2SO4) and filtered through a thin pad of hydrous magnesium silicate and the filtrate concentrated to dryness. The residue is chromatographed on thick layer silica gel plates with ethyl acetate-hexane (1:1) as solvent to give 0.100 g of white solid, m.p. 230°-240° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05733905
출처 데이터셋uspto-grants-1998_03
ORD IDord-19075005e7214f38bc08e67939d9a779
출처 메모uspto-grants-1998_03