Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993862Generated: November 1, 2026

Butyl isocyanate → N-(Butylamino)carbonyl-3-(4-imidazol-1-ylmethylphenyl)-5-iso-butylthiophene-2-sulfonamide

https://huagongshe.com/reaction/1993862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl isocyanateHCID 8110—
ReactantSodium HydroxideHCID 14798—
Reactant3(4-Imidazol-1-ylmethylphenyl)5-iso-butylthiophene-2 sulfonamideHCID 11394744—
Reactant3-(4-Imidazol-1-ylmethylphenyl)-5-iso-butyl-N-tert-butylthiophene-2-sulfonamideHCID 11419042—
SolventAcetoneHCID 180—
SolventEthyl AcetateHCID 8857—
ProductN-(Butylamino)carbonyl-3-(4-imidazol-1-ylmethylphenyl)-5-iso-butylthiophene-2-sulfonamideHCID 1022733733%

Reaction Steps

The crude product from step (c) above was dissolved in acetone (5 mL) under N2 (g). NaOH (0.20 mL, 1M, 0.20 mmol) was added to the mixture, which was then stirred for 10 min. Butyl isocyanate (109 μL, 0.97 mmol) was then added and the mixture was stirred overnight 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. Purification using column chromatography with CHCl3:MeOH (10:1) as eluent yielded the title compound (15.1 mg, 0.032 mmol) in 33% yield (from 3-(4-imidazol-1-ylmethylphenyl)-5-iso-butylthiophene-2-sulfonic acid tert-butylamide).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652054B2
Source datasetuspto-grants-2010_01
ORD IDord-ab35e8ef35b74e66bce8504bfa524795
Source noteuspto-grants-2010_01