돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 400504생성일: 2026년 10월 24일

2-Fluoroaniline → N-(2-fluorophenyl)-3-[(8aS)-hexahydropyrrolo[1,2-a]pyrazin-2(1H)-ylcarbonyl]benzenesulfonamide

https://huagongshe.com/ko/reaction/400504

반응식

참여 물질

역할이름HCID투입량
반응물2-FluoroanilineHCID 9584—
반응물Benzoyl chloride, 3-(chlorosulfonyl)-HCID 77671—
반응물(6S)-1,4-Diazabicyclo(4.3.0)nonaneHCID 781249—
용매DichloromethaneHCID 6344—
생성물N-(2-fluorophenyl)-3-[(8aS)-hexahydropyrrolo[1,2-a]pyrazin-2(1H)-ylcarbonyl]benzenesulfonamideHCID 46851310—

반응 단계

To 3-(chlorosulfonyl)benzoyl chloride (0.521 g, 2.18 mmol) in anhydrous dichloromethane (10 mL) was added (S)-octahydropyrrolo[1,2-a]pyrazine (0.250 g, 1.98 mmol) in dichloromethane (4 mL) slowly over 10 minutes at room temperature. The mixture was stirred at room temperature for 5 hours. Then 2-fluoroaniline (1.54 g, 13.87 mmol) was added. The mixture was stirred at room temperature overnight and then concentrated. The residue was purified by chromatography on silica gel (dichloromethane, then methanol/dichloromethane=1:10) to give the titled compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08741899B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-d942abd221534db3bb1ed208b2cab874
출처 메모uspto-grants-2014_06