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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 865105Generated: November 3, 2026

Bromine → HCID 19417722, compound

https://huagongshe.com/reaction/865105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantHCID 19417724HCID 19417724—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19417722HCID 19417722—

Reaction Steps

0.1 ml of bromine was added dropwise to a solution of 0.47 g of 7-benzoyloxy-1-indanone in tetrahydrofuran (10 ml) at room temperature, and the mixture was stirred for 30 minutes. To 7-benzoyloxy-2-bromo-1-indanone obtained by evaporation of the solvent was added 15 ml of 2-propanol and 0.33 g of 4-imidazolylthioacetamide hydrochloride, followed by 2.5 hours of heating under reflux. After cooling and evaporation of the solvent, the residue was mixed with ethyl acetate, and extracted with 1N hydrochloric acid. The aqueous layer was neutralized with sodium bicarbonate and then extracted with chloroform. The organic layer was dried over anhydrous magnesium sulfate and the solvent was evaporated. The residual 4-benzoyloxy-2-(4-imidazolylmethyl)-8H-indeno[1,2-d]thiazole was dissolved in 10 ml of methanol, to the solution was added 1 ml of 5N aqueous sodium hydroxide solution and then stirred at room temperature for 15 minutes. After acidifying with 1N hydrochloric acid, the reaction solution was neutralized with sodium bicarbonate, and extracted with chloroform-methanol, and then the extract was dried over anhydrous magnesium sulfate. After evaporation of the solvent, the resultant crude crystals were recrystallized from ethanol to obtain 55 mg of 4-hydroxy-2-(4-imidazolylmethyl)-8H-indeno[1,2-d]thiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05565479
Source datasetuspto-grants-1996_10
ORD IDord-45b844e4211f4a68be5cbd6124fac8c1
Source noteuspto-grants-1996_10