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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (6-Bromo-imidazo[1,2-a]pyridin-2-yl)-carbamic acid phenyl ester | HCID 59251768 | — |
| Reactant | 2-(2-isopropyl-2H-tetrazol-5-yl)-ethylamine hydrochloride | HCID 66986243 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 1-(6-Bromo-imidazo[1,2-a]pyridin-2-yl)-3-[2-(2-isopropyl-2H-tetrazol-5-yl)-ethyl]-urea | HCID 59251873 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08053574B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-268bf53b7ef243cd874d0e916aca8792 |
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| Source note | uspto-grants-2011_11 |
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