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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555980Generated: October 31, 2026

Water → 1-[2-(2-Isopropyl-2H-tetrazol-5-yl)-ethyl]-3-[6-(6-methoxy-pyridin-3-yl)-imidazo[1,2-a]pyridin-2-yl]-urea

https://huagongshe.com/reaction/555980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant[6-(6-Methoxy-pyridin-3-yl)-imidazo[1,2-a]pyridin-2-yl]carbamic acid phenyl esterHCID 66986116—
Reactant2-(2-isopropyl-2H-tetrazol-5-yl)-ethylamine hydrochlorideHCID 66986243—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product1-[2-(2-Isopropyl-2H-tetrazol-5-yl)-ethyl]-3-[6-(6-methoxy-pyridin-3-yl)-imidazo[1,2-a]pyridin-2-yl]-ureaHCID 25176428—

Reaction Conditions

Temperature80 °C

Reaction Steps

Triethylamine (0.54 ml, 3.26 mmol) is added to a stirred mixture of [6-(6-methoxy-pyridin-3-yl)-imidazo[1,2-a]pyridin-2-yl]carbamic acid phenyl ester (Intermediate C) (0.587 g, 1.63 mmol) and 2-(2-isopropyl-2H-tetrazol-5-yl)-ethylamine hydrochloride (Intermediate D1)(0.275 g, 1.96 mmol) in NMP (5 ml). The resulting mixture is stirred at 80° C. for 2 hours and then allowed to cool to room temperature. Water (100 ml) is added and the resulting grey suspension is collected by filtration and dried in a vacuum oven to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053574B2
Source datasetuspto-grants-2011_11
ORD IDord-be7ba172d48247248528b8bb39cec30e
Source noteuspto-grants-2011_11