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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555993Generated: October 27, 2026

Triethylamine → 1-(6-Bromo-imidazo[1,2-a]pyridin-2-yl)-3-[2-(2-isopropyl-2H-tetrazol-5-yl)-ethyl]-urea

https://huagongshe.com/reaction/555993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(6-Bromo-imidazo[1,2-a]pyridin-2-yl)-carbamic acid phenyl esterHCID 59251768—
Reactant2-(2-isopropyl-2H-tetrazol-5-yl)-ethylamine hydrochlorideHCID 66986243—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product1-(6-Bromo-imidazo[1,2-a]pyridin-2-yl)-3-[2-(2-isopropyl-2H-tetrazol-5-yl)-ethyl]-ureaHCID 59251873—

Reaction Conditions

Temperature80 °C

Reaction Steps

Triethylamine (0.15 ml, 1.1 mmol) is added to a stirred mixture of (6-bromo-imidazo[1,2-a]pyridin-2-yl)-carbamic acid phenyl ester (Intermediate B1)(0.30 g, 0.90 mmol) and 2-(2-isopropyl-2H-tetrazol-5-yl)-ethylamine hydrochloride (Intermediate D1)(0.207 g, 1.1 mmol) in NMP (3 ml). The reaction mixture is stirred at 80° C. for 2 hours, cooled and diluted with water (100 ml) resulting in a grey precipitate. The solid is collected by filtration and dried in a vacuum oven to afford the title compound. [MH+ 395.09]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053574B2
Source datasetuspto-grants-2011_11
ORD IDord-268bf53b7ef243cd874d0e916aca8792
Source noteuspto-grants-2011_11