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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 405802생성일: 2026년 10월 24일

Water → Tert-butyl 3-((3-(3-(imidazo[1,2-a]pyridine-3-carboxamido)-4-methylphenyl)-1,2,4-oxadiazol-5-yl)methyl)azetidine-1-carboxylate

https://huagongshe.com/ko/reaction/405802

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Bis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
반응물2-(1-(Tert-butoxycarbonyl)azetidin-3-yl)acetic acidHCID 11095989—
반응물N-(5-(N'-hydroxycarbamimidoyl)-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamideHCID 86677441—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물Tert-butyl 3-((3-(3-(imidazo[1,2-a]pyridine-3-carboxamido)-4-methylphenyl)-1,2,4-oxadiazol-5-yl)methyl)azetidine-1-carboxylateHCID 71281398—

반응 조건

온도125 °C

반응 단계

Carbonyl diimidazole (CDI) (52.0 mg, 0.32 mmol) was added to a stirred solution of 2-(1-(tert-butoxycarbonyl)azetidin-3-yl)acetic acid (69.0 mg, 0.32 mmol) in NMP (1.0 mL). After 20 minutes, N-(5-(N′-hydroxycarbamimidoyl)-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamide (9) (49.5 mg, 0.16 mmol) was added in one portion and the resulting solution was stirred for 30 minutes before it was heated at 125° C. for 15 minutes in a microwave reactor. The reaction mixture was added dropwise to water (20 mL) with stirring. The precipitate was filtered and dried to give tert-butyl 3-((3-(3-(imidazo[1,2-a]pyridine-3-carboxamido)-4-methylphenyl)-1,2,4-oxadiazol-5-yl)methyl)azetidine-1-carboxylate (54). MS m/z 489.2 (M+1)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08754071B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-6cdf3e92c7e2492dab844346282e1328
출처 메모uspto-grants-2014_06