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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280799Generated: October 26, 2026

Sodium hydride → isopropyl N-(4-pyridylmethyl)-2-bromo-4-methyl-5-imidazole carboxylate

https://huagongshe.com/reaction/280799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-(Chloromethyl)pyridineHCID 74571—
ReactantHCID 178432453HCID 178432453—
SolventTetrahydrofuranHCID 8028—
Productisopropyl N-(4-pyridylmethyl)-2-bromo-4-methyl-5-imidazole carboxylateHCID 1363330792%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 195 milligrams (mg) (8.13 mM) of sodium hydride in 20 ml of anhydrous tetrahydrofuran was added, in portions, 2 g (8.13 mM) of isopropyl 2-bromo-4-methyl-5-imidazolecarboxylate. The resulting suspension was cooled to 0° C. and 1.03 g (8.13 mM) of 4-chloromethylpyridine was added. The reaction mixture was stirred overnight at 50° C. The precipitated sodium chloride was removed by filtration and concentration in vacuo of the filtrate gave 2.5 g (92%) of isopropyl N-(4-pyridylmethyl)-2-bromo-4-methyl-5-imidazole carboxylate as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04591377
Source datasetuspto-grants-1986_05
ORD IDord-dbb495aba34848dc857773c0f1cfbd27
Source noteuspto-grants-1986_05