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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644854Generated: November 2, 2026

Sodium Hydroxide → N-butylsulfonyl-3-(4-imidazol-1-ylmethylphenyl)-5-iso-butylthiophene-2-sulfonamide

https://huagongshe.com/reaction/1644854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant1-Butanesulfonyl chlorideHCID 75430—
Reactant3(4-Imidazol-1-ylmethylphenyl)5-iso-butylthiophene-2 sulfonamideHCID 11394744—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductN-butylsulfonyl-3-(4-imidazol-1-ylmethylphenyl)-5-iso-butylthiophene-2-sulfonamideHCID 10300357—

Reaction Steps

Crude 3-(4-imidazol-1-ylmethylphenyl)-5-iso-butylthiophene-2-sulfonamide (prepared according to the procedure described in Example 10(c) above) was dissolved in THF (3 mL) under N2 (g). NaOH (1.0 mL, 1M, 1.0 mmol) was added to the mixture, which was then stirred for 10 min. Butanesulfonyl chloride (45 μL, 0.35 mmol) was then added, and the mixture was stirred for 24 h at room temperature. The reaction mixture was then diluted with ethyl acetate (150 mL) and washed with water and brine. The organic phase was dried over MgSO4 and the solvent was removed in vacuo. The crude product was recrystallised from acetone to yield the title compound (31.7 mg, 0.064 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124638B2
Source datasetuspto-grants-2012_02
ORD IDord-45fe013a3d1e4c489420a0c51fc6d1b9
Source noteuspto-grants-2012_02