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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222580Generated: October 31, 2026

Benzyl Bromide → HCID 178518536, compound

https://huagongshe.com/reaction/2222580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantHCID 178518550HCID 178518550—
SolventMethanolHCID 887—
SolventSodium HydroxideHCID 14798—
ProductHCID 178518536HCID 178518536—

Reaction Steps

To a solution of 5-(1H-pyrrolo[2,3-b]pyridin-3-ylmethylene)-2-thioxoimidazolidin-4-one (500 mg, 2.05 mmol) in 12.6% aq. NaOH (1 mL) and methanol (5 mL), benzyl bromide (430 mg, 2.5 mmol) was added and the reaction mixture stirred at RT for 18 h. Most of the solvent was distilled out and the precipitate was filtered and washed first with water, then with diethylether and dried. The crude material was purified by flash chromatography on silica gel (eluant: dichloromethane/methanol 15:1). Obtained the desired (5Z)-2-(benzylthio)-5-(1H-pyrrolo[2,3-b]pyridin-3-ylmethylene)-3,5-dihydro-4H-imidazol-4-one, as a yellow solid (700 mg, 2 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07371862B2
Source datasetuspto-grants-2008_05
ORD IDord-0c7a28345d734ba290ae1ecfb3edc8bf
Source noteuspto-grants-2008_05