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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18431생성일: 2026년 10월 27일

Triethylamine → N-(5-{3-[(2-oxo-1-pyrrolidinyl)methyl]phenyl}-2,3-dihydro-1H-inden-2-yl)-2-propanesulfonamide

https://huagongshe.com/reaction/18431

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Potassium CarbonateHCID 11430—
반응물4-Chlorobutyryl chlorideHCID 78370—
반응물N-{5-[3-(aminomethyl)phenyl]-2,3-dihydro-1H-inden-2-yl}-2-propanesulfonamideHCID 11515729—
용매DichloromethaneHCID 6344—
생성물N-(5-{3-[(2-oxo-1-pyrrolidinyl)methyl]phenyl}-2,3-dihydro-1H-inden-2-yl)-2-propanesulfonamideHCID 1168304519.4%

반응 단계

A solution of N-{5-[3-(aminomethyl)phenyl]-2,3-dihydro-1H-inden-2-yl}-2-propanesulfonamide (69 mg, 0.2 mmol) in dichloromethane (5 ml) was treated with triethylamine (40 mg, 0.4 mmol), followed by 4-chlorobutanoyl chloride (32 mg, 0.22 mmol) and the whole mix stirred at room temperature under argon for 1 h. The reaction mix was evaporated under reduced pressure to remove the dichloromethane and then dimethylformamide was added (5 ml) followed by potassium carbonate (60 mg, 0.43 mmol) and the mix stirred at 100° C. for 2 h. The reaction mix was cooled then partitioned between dichloromethane and 0.5M hydrochloric acid, and the organic layer was evaporated under reduced pressure to give a brown oil which was purified by column chromatography on a 1 g SCX column eluting from 0-50% ethyl acetate in 40-60° C. petroleum ether to give the title compound as a beige solid (16 mg, 19%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741351B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-9a8a09a287e142e79aaaadf407bc6de2
출처 메모uspto-grants-2010_06