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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1871944Generated: November 1, 2026

Acetyl chloride → 1-Acetyl-2-{[[4-(2-furylmethylthio)-3-methyl-2-pyridinyl]methyl]thio}benzimidazole

https://huagongshe.com/reaction/1871944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
Reactant2-{[[4-(2-Furylmethylthio)-3-methyl-2-pyridinyl]methyl]thio}-1H-benzimidazoleHCID 9799366—
SolventDichloromethaneHCID 6344—
Product1-Acetyl-2-{[[4-(2-furylmethylthio)-3-methyl-2-pyridinyl]methyl]thio}benzimidazoleHCID 1869000797%

Reaction Conditions

Temperature20 °C

Reaction Steps

2-{[[4-(2-Furylmethylthio)-3-methyl-2-pyridinyl]methyl]thio}-1H-benzimidazole (5.0 mmol) is suspended in anhydrous methylene chloride (50 ml), triethylamine (11 mmol and acetyl chloride (8 mmol) are added and the mixture is stirred at 20° C. for 20 h. The clear reaction solution is washed with sodium bicarbonate solution and water, dried over magnesium sulfate and concentrated and the residue is crystallized by addition of diisopropyl ether. The title compound is obtained as a colorless powder; m.p. 168-169° C. (decomp.); yield: 97% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06107312
Source datasetuspto-grants-2000_08
ORD IDord-e8aa1f19f88a449eb8209ee9a52528c0
Source noteuspto-grants-2000_08