Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811017Generated: November 1, 2026

Diisopropylethylamine → N-(3-bromo-2-methylphenyl)-1H-imidazole-2-carboxamide

https://huagongshe.com/reaction/1811017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Bromo-o-toluidineHCID 123538—
ReactantHOAtHCID 181649—
Reactant1H-Imidazole-2-carboxylic acidHCID 574321—
Solvent1,2-DichloroethaneHCID 11—
SolventTetrahydrofurane dichloromethaneHCID 21919333—
ProductN-(3-bromo-2-methylphenyl)-1H-imidazole-2-carboxamideHCID 66606432—

Reaction Steps

Step 1 A solution of 3-bromo-2-methylaniline (0.63 g, 3.39 mmol), 1H-imidazole-2-carboxylic acid (0.455 g, 4.06 mmol), HOAT (0.830 g, 6.10 mmol), and EDC (1.298 g, 6.77 mmol) in 2:1 DCM-THF (100 mL) was treated with DIEA (1.774 mL, 10.16 mmol) and stirred at rt overnight. Additional 1H-imidazole-2-carboxylic acid (0.6 eq, 0.228 g), EDC (0.64 g), HOAT (0.41 g), and DIEA (0.8 mL) were added and the mixture was stirred at rt for 6 days. The mixture was partitioned between NaHCO3 (aq) and DCM, and the organic phase was washed with brine, dried and concentrated. The residue was purified by column chromatography (eluting with a gradient from DCM to 94:6 DCM-methanol) to provide N-(3-bromo-2-methylphenyl)-1H-imidazole-2-carboxamide as a solid (80% purity, 0.76 g, 64%). Mass spectrum m/z 280, 282 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362065B2
Source datasetuspto-grants-2013_01
ORD IDord-a6e3ae5dd0264e00ba6332cfb14d2257
Source noteuspto-grants-2013_01