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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 536320생성일: 2026년 10월 25일

Pyridine → 4-Fluoro-N-[2-methyl-6-((2S,3'R)-2-methyl-[1,3']bipyrrolidinyl-1'-yl)-pyridin-3-yl]-benzenesulfonamide

https://huagongshe.com/reaction/536320

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Tris(hydroxymethyl)aminomethaneHCID 6503—
반응물4-Fluorobenzenesulfonyl chlorideHCID 9588—
반응물2-methyl-6-[(3R)-3-[(2S)-2-methylpyrrolidin-1-yl]pyrrolidin-1-yl]pyridin-3-amineHCID 67480461—
용매1,2-DichloroethaneHCID 11—
생성물4-Fluoro-N-[2-methyl-6-((2S,3'R)-2-methyl-[1,3']bipyrrolidinyl-1'-yl)-pyridin-3-yl]-benzenesulfonamideHCID 5459715718.3%

반응 단계

To a solution of 2-methyl-6-[(3R)-3-[(2S)-2-methylpyrrolidin-1-yl]pyrrolidin-1-yl]pyridin-3-amine (22.7 mg, 0.09 mmol) in DCE (1 mL) was added pyridine (0.22 mL, 2.7 mmol) followed by a solution of 4-fluoro-benzenesulfonyl chloride (53 mg, 0.27 mmol) in DCE (1 mL) and stirred at ambient temperature for 5 hours. To this mixture was then added trisamine resin (200 mg, 0.8 mmol, 4 mmol/g loading), stirred for 30 min, filtered and concentrated to afford a crude solid which was purified by flash column chromatography (5% 7N NH3 in MeOH/CH2Cl2) to obtain 6.9 mg of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08859588B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-6e70391e63db482a90bcbb12d4d30b5d
출처 메모uspto-grants-2014_10