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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 570312생성일: 2026년 10월 26일

Methanesulfonyl chloride → (3-(3-(Imidazo[1,2-a]pyridine-3-carboxamido)-4-methylphenyl)-1,2,4-oxadiazol-5-yl)methyl methanesulfonate

https://huagongshe.com/reaction/570312

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonyl chlorideHCID 31297—
반응물DiisopropylethylamineHCID 81531—
반응물N-(5-(5-(hydroxymethyl)-1,2,4-oxadiazol-3-yl)-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamideHCID 71280825—
용매DichloromethaneHCID 6344—
생성물(3-(3-(Imidazo[1,2-a]pyridine-3-carboxamido)-4-methylphenyl)-1,2,4-oxadiazol-5-yl)methyl methanesulfonateHCID 8667744770.2%

반응 단계

To a solution of N-(5-(5-(hydroxymethyl)-1,2,4-oxadiazol-3-yl)-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamide (43) (210 mg, 0.6 mmol) and DIEA (0.32 mL, 1.8 mmol) in DCM (5 mL) was added MsCl (138 mg, 1.2 mmol). The mixture was stirred at room temperature for 10 minutes then subjected to standard aqueous work up. The crude product was purified by silica chromatography to yield (3-(3-(imidazo[1,2-a]pyridine-3-carboxamido)-4-methylphenyl)-1,2,4-oxadiazol-5-ylmethyl methanesulfonate (44) (180 mg, 70% yield). MS m/z 428.1 (M+1)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09023839B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-1409e36b76ed41fc83a5272aa2b662bd
출처 메모uspto-grants-2015_05