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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 405790생성일: 2026년 10월 26일

Chloroacetic anhydride → N-(5-(5-(chloromethyl)-1,2,4-oxadiazol-3-yl)-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamide

https://huagongshe.com/reaction/405790

반응식

참여 물질

역할이름HCID투입량
반응물Chloroacetic anhydrideHCID 10946—
반응물N-(5-(N'-hydroxycarbamimidoyl)-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamideHCID 86677441—
용매WaterHCID 962—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물N-(5-(5-(chloromethyl)-1,2,4-oxadiazol-3-yl)-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamideHCID 86677445—

반응 조건

온도110 °C

반응 단계

A mixture of N-(5-(N′-hydroxycarbamimidoyl)-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamide (9) (500 mg, 1.62 mmol) and 2-chloroacetic anhydride (553 mg, 3.23 mmol) in anhydrous NMP (10 mL) was heated in the microwave at 110° C. for 12 minutes. The crude was diluted with water and extracted with ethyl acetate. The organic was washed with a water/brine mixture and dried over anhydrous sodium sulfate. The solvent was concentrated and the crude product was purified by silica chromatography to yield N-(5-(5-(chloromethyl)-1,2,4-oxadiazol-3-yl)-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamide (38). MS m/z 378.9 (M+1)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08754071B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-ee9e4dcc2cdd4e24bcfc37014fb658c7
출처 메모uspto-grants-2014_06