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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8622생성일: 2026년 10월 23일

Chlorosulfonic acid → 4-Ethoxy-3-(8-cyclopentyl-6-methyl-4-oxo-3,4-dihydro-imidazol[1,5-a][1,3,5]-triazin-2-yl)-benzenesulfonyl chloride

https://huagongshe.com/ko/reaction/8622

반응식

참여 물질

역할이름HCID투입량
반응물Chlorosulfonic acidHCID 24638—
반응물8-Cyclopentyl-2-(2-ethoxy-phenyl)-6-methyl-3H-imidazo[1,5-a][1,3,5]triazin-4-oneHCID 135723513—
용매DichloromethaneHCID 6344—
생성물4-Ethoxy-3-(8-cyclopentyl-6-methyl-4-oxo-3,4-dihydro-imidazol[1,5-a][1,3,5]-triazin-2-yl)-benzenesulfonyl chlorideHCID 135723515—

반응 단계

372.3 mg (1.1 mmol) of 8-cyclopentyl-2-(2-ethoxy-phenyl)-6-methyl-3H-imidazo[1,5-a][1,3,5]triazin-4-one (example IX) are added in portions to 0.66 ml (9.9 mmol) of ice-cooled chlorosulfonic acid. The mixture is subsequently stirred overnight at room temperature before being diluted with dichloromethane and poured onto ice water. The organic phase is separated off. The aqueous phase is extracted once again with dichloromethane and the organic phases are combined, dried and evaporated.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091203B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-6f110095d41b437f9aec3433c29d3d1d
출처 메모uspto-grants-2006_08