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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452747Generated: October 30, 2026

Acetic Acid → HCID 68663473, compound

https://huagongshe.com/reaction/452747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethylformamideHCID 6228—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantHCID 68664090HCID 68664090—
SolventPyridineHCID 1049—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68663473HCID 686634733.8%

Reaction Steps

A solution of acetic acid (57 μl, 1.00 mmol) and N,N′-carbonyldiimidazole (195 mg, 1.20 mmol) in tetrahydrofuran (20 mL) was stirred at room temperature for 1 hr. To this reaction mixture were added 1-[4-(methylsulfinyl)phenyl]-1H-benzimidazole-6-carbohydrazide (314 mg, 1.00 mmol) and N,N-dimethylformamide (5 mL), and the resulting mixture was stirred overnight. To this reaction mixture was added a solution of p-toluenesulfonyl chloride (381 mg, 2.00 mmol) in pyridine (5 mL), and the resulting mixture was stirred at 80° C. for 24 hr. After cooling, the reaction mixture was diluted with chloroform, washed with 1M hydrochloric acid, saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (hexane/ethyl acetate=4/1-0/1) and recrystallized from hexane/ethyl acetate to give the title compound (12 mg, yield 3.8%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492378B2
Source datasetuspto-grants-2013_07
ORD IDord-e86a4db125e349b7873414e090354639
Source noteuspto-grants-2013_07