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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1984537Generated: November 1, 2026

2-Dimethylaminopyridine → 1-[(5-Chlorothien-2-yl)sulfonyl]-3-[2-(dimethylamino)ethyl]-1,3-dihydro-2H-benzimidazol-2-one

https://huagongshe.com/reaction/1984537

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-DimethylaminopyridineHCID 21885—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Chlorothiophene-2-sulfonyl chlorideHCID 2733925—
Reactant1-[2-(Dimethylamino)ethyl]-1,3-dihydrobenzimidazol-2-oneHCID 14894678—
SolventTetrahydrofuranHCID 8028—
Product1-[(5-Chlorothien-2-yl)sulfonyl]-3-[2-(dimethylamino)ethyl]-1,3-dihydro-2H-benzimidazol-2-oneHCID 11429094—

Reaction Steps

A solution of 1-[2-(dimethylamino)ethyl]-1,3-dihydrobenzimidazol-2-one (20 mg, 0.1 mmol) in THF at room temperature is treated with (5-chlorothien-2-yl)sulfonyl chloride (26 mg, 0.12 mmol) followed by diisopropylethylamine (25 uL, 0.2 mmol) and dimethylaminopyridine (5 mg), stirred at room temperature for 16 hours and concentrated in vacuo. The resultant residue is dissolved in a mixture of dimethylsulfoxide, methanol and water and purified by Gilson1 preparative HPLC to give the title product, 16 mg, [M+H] 386, retention time (RT) 2.83 minutes. 1Gilson Preparative HPLC conditions: Gilson Preparative HPLC system; YMC Pro C18, 20 mm×50 mm ID, 5 uM column; 2 mL injection; Solvent A: 0.02% TFA/water; Solvent B:0.02% TFA/acetonitrile; Gradient: Time 0: 95% A; 2 min: 95% A; 14 min: 10% A, 15 min: 10% A, 16 min: 95% A; Flow rate 22.5 mL/min; Detection: 254 nm DAD.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544701B2
Source datasetuspto-grants-2009_06
ORD IDord-b202429ebe3943e18864e1e2ed012ecb
Source noteuspto-grants-2009_06