돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 572209생성일: 2026년 10월 25일

Triethylamine → N-(3-{(1S)-1-[(6-chloropyrazin-2-yl)amino]ethyl}phenyl)pyridine-3-sulfonamide

https://huagongshe.com/reaction/572209

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Pyridine-3-sulfonyl chloride hydrochlorideHCID 12571517—
반응물(S)-N-(1-(3-aminophenyl)ethyl)-6-chloropyrazin-2-amineHCID 25218447—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물N-(3-{(1S)-1-[(6-chloropyrazin-2-yl)amino]ethyl}phenyl)pyridine-3-sulfonamideHCID 2521845028.2%

반응 단계

To a suspension of pyridine-3-sulfonylchloride hydrochloride (94 mg, 0.44 mmol) and N-[(1S)-1-(3-aminophenyl)ethyl]-6-chloropyrazin-2-amine (100 mg, 0.4 mmol) in dichloromethane (5 mL) was added triethylamine (0.17 mL, 1.2 mmol) dropwise at room temperature and the mixture was stirred for 17 hours. After this time the mixture was diluted with ethyl acetate (20 mL), washed successively with saturated aqueous sodium hydrogen carbonate (2×20 mL) and brine (20 mL), dried (Na2SO4) and concentrated under reduced pressure to give a yellow oil which was purified by flash chromatography (silica, ethyl acetate/hexanes) to give N-(3-{(1S)-1-[(6-chloropyrazin-2-yl)amino]ethyl}phenyl)pyridine-3-sulfonamide (44 mg, 28%) as a pale yellow foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09029386B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-7a9cede1e5ee4d758212fa9731856dc6
출처 메모uspto-grants-2015_05