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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885458Generated: October 30, 2026

Benzenesulfonyl chloride → HCID 58094712, compound

https://huagongshe.com/reaction/885458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantHCID 923834HCID 923834—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductHCID 58094712HCID 58094712—

Reaction Conditions

Temperature100 °C

Reaction Steps

To (4-chloro-phenyl)-(1-methyl-1H-benzimidazol-2-yl)-amine (258 mg, 1.0 mmol) in anhydrous pyridine (4 mL) at room temperature was added benzenesulfonyl chloride (706.5 mg, 4.0 mmol). The resulting mixture was heated to 100° C. in a microwave reactor for 1 h. The resulting mixture was then diluted with EtOAc, washed with 1 N HCl and the organic layer was dried over Na2SO4, filtered, and concentrated in vacuo. The resultant residue was purified by flash column chromatography (SiO2), eluting with a hexanes-EtOAc gradient to yield the title compound as a crude residue, which was dissolved in ether containing 2.0M hydrogen chloride, and then concentrated in vacuo to yield the title compound as its corresponding HCl salt. MS 398 (M+1)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242157B2
Source datasetuspto-grants-2012_08
ORD IDord-dd12bb190df44031a7d2dea0cdaff579
Source noteuspto-grants-2012_08