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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 865108Generated: October 27, 2026

Imidazole → 2-(1-Imidazolylmethyl)naphtho[1,2-d]thiazole

https://huagongshe.com/reaction/865108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantSodium hydrideHCID 24758—
Reactant2-Bromomethylnaphtho[1,2-d]thiazoleHCID 18941095—
SolventTetrahydrofuranHCID 8028—
Product2-(1-Imidazolylmethyl)naphtho[1,2-d]thiazoleHCID 67771527100%

Reaction Steps

0.06 g of sodium hydride (60%) was added to a solution of 0.10 g of imidazole in tetrahydrofuran (30 ml). After 30 minutes of stirring at room temperature, a solution of 2-bromomethylnaphtho[1,2-d]thiazole in tetrahydrofuran (10 ml) was added to the solution. After stirring at room temperature for 1 hour and evaporation of the solvent, the residue was partitioned between 1N hydrochloric acid and ethyl acetate. The organic layer was extracted with 1N hydrochloric acid. The combined aqueous layer was neutralized with sodium bicarbonate and then extracted with chloroform. After drying over anhydrous magnesium sulfate, the solvent was evaporated to obtain 0.27 g (100%) of 2-(1-imidazolylmethyl)naphtho[1,2-d]thiazole. This free base was dissolved in methanol and mixed with 0.10 g of fumaric acid to effect crystallization to give 0.32 g of fumarate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05565479
Source datasetuspto-grants-1996_10
ORD IDord-d2b59979e3774f9bae72504a35d84ec3
Source noteuspto-grants-1996_10