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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 870372생성일: 2026년 10월 26일

4-((S)-2-Fluoro-1-methyl-ethyl)-benzenesulfonyl chloride → N-{7-[4-((S)-2-Fluoro-1-methyl-ethyl)-benzenesulfonylamino]-3,4-dihydro-2H-pyrano[3,2-b]pyridin-3-yl}-propionamide

https://huagongshe.com/reaction/870372

반응식

참여 물질

역할이름HCID투입량
반응물4-((S)-2-Fluoro-1-methyl-ethyl)-benzenesulfonyl chlorideHCID 53628600—
반응물N-(7-amino-3,4-dihydro-2H-pyrano[3,2-b]pyridin-3-yl)propionamideHCID 68912527—
용매Pyridine methylene chlorideHCID 21875418—
생성물N-{7-[4-((S)-2-Fluoro-1-methyl-ethyl)-benzenesulfonylamino]-3,4-dihydro-2H-pyrano[3,2-b]pyridin-3-yl}-propionamideHCID 68916577—

반응 단계

Following the same procedure as described in example 31.5, a portion of crude N-(7-amino-3,4-dihydro-2H-pyrano[3,2-b]pyridin-3-yl)-propionamide (95 mg, 0.43 mmol) in CH2Cl2/pyridine 9/1 (10 ml) was treated with 4-((S)-2-fluoro-1-methyl-ethyl)benzenesulfonyl chloride (132 mg, 0.55 mmol). Purification by flash column chromatography (CH2Cl2:MeOH, 97:3) gave the title compound (100 mg, 55% for step 31.4 and this step) as a gum.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08969552B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-c0f532e3a84147a5b3e01792998d92fe
출처 메모uspto-grants-2015_03