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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045426Generated: October 26, 2026

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/reaction/1045426

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
Reactant2-(1-(Tert-butoxycarbonyl)azetidin-3-yl)acetic acidHCID 11095989—
ReactantN-(5-(N'-hydroxycarbamimidoyl)-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamideHCID 86677441—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductTert-butyl 3-((3-(3-(imidazo[1,2-a]pyridine-3-carboxamido)-4-methylphenyl)-1,2,4-oxadiazol-5-yl)methyl)azetidine-1-carboxylateHCID 71281398—

Reaction Conditions

Temperature125 °C

Reaction Steps

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)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569283B2
Source datasetuspto-grants-2013_10
ORD IDord-3a0373ee6d984cf898333729b8e00f0b
Source noteuspto-grants-2013_10