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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 455140Generated: October 31, 2026

Hydroxyamine hydrochloride → N-hydroxy-3-((2-phenylimidazo[1,2-a]pyridin-3-yl)-methyl)-1,2,4-oxadiazole-5-carboxamide

https://huagongshe.com/reaction/455140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 44539338HCID 44539338—
ReactantHCID 67028744HCID 67028744—
ProductN-hydroxy-3-((2-phenylimidazo[1,2-a]pyridin-3-yl)-methyl)-1,2,4-oxadiazole-5-carboxamideHCID 86655128—

Reaction Steps

The title compound was prepared in the same fashion as that for compound 222 from ethyl 3-((2-(4-chlorophenyl)imidazo[1,2-a]pyridin-3-yl)methyl)-1,2,4-oxadiazole-5-carboxylate and hydroxylamine hydrochloride. m/e+=370 (M+H+). 1H NMR (400 MHz, in DMSO-d6): δ 8.43-8.41 (1H, D, d, J=7.2 Hz, ArH), δ 8.31 (1H, D, s, ArH), δ 7.88-7.86 (2H, D, d, J=8.4 Hz, ArH), δ 7.65-7.62 (1H, D, d, J=9.2 Hz, ArH), δ 7.57-7.54 (1H, D, d, J=8.4 Hz, ArH), δ 7.35-7.31 (1H, D, t, J=8.0, ArH), δ 7.04-7.00 (1H, D, t, J=8.0, ArH), and δ 4.62 (2H, D, s, CH2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08497278B2
Source datasetuspto-grants-2013_07
ORD IDord-2ec0d0a4d83746d0ab3255cfd83f2ee2
Source noteuspto-grants-2013_07