Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241013Generated: October 30, 2026

Isobutyl chloroformate → isobutyl 6-bromo-2-methyl-1H-imidazo[4,5-b]pyridine-1-carboxylate

https://huagongshe.com/reaction/241013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyl chloroformateHCID 62365—
ReactantDiisopropylethylamineHCID 81531—
Reactant6-bromo-2-methyl-1H-imidazo(4,5-b)pyridineHCID 1958572—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Productisobutyl 6-bromo-2-methyl-1H-imidazo[4,5-b]pyridine-1-carboxylateHCID 6682007646%

Reaction Steps

To a solution of 6-bromo-2-methyl-1H-imidazo[4,5-b]pyridine (3.40 g, 16.0 mmol) and diisopropylethylamine (6.5 mL, 65 mmol) in N,N-dimethylformamide (20 mL) cooled in an ice bath was added dropwise isobutyl chloroformate (2.51 mL, 19.2 mmol) and the mixture was warmed to room temperature. After 1 hour the reaction was diluted with ethyl acetate (80 mL) and washed with water (60 mL), 10% aqueous citric acid (40 mL) and brine (20 mL). The organic phase was dried over anhydrous sodium sulfate, filtered and concentrated to a slurry. The residue was triturated diethyl ether (100 mL) and the solid isolated by filtration to give isobutyl 6-bromo-2-methyl-1H-imidazo[4,5-b]pyridine-1-carboxylate (2.3 g, 46% yield). MS (EI) for C12H14BrN3O2: 313 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648066B2
Source datasetuspto-grants-2014_02
ORD IDord-2f4846d5d4d64fdcb3c7c8c86601ecab
Source noteuspto-grants-2014_02