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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786588Generated: October 31, 2026

2-Methylbenzenesulfonamide → N-[4-(Biphenyl-4-yloxymethyl)-5-methyl-furan-2-carbonyl]-2-methyl-benzenesulphonamide

https://huagongshe.com/reaction/1786588

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylbenzenesulfonamideHCID 6924—
Reactant4-(Biphenyl-4-yloxymethyl)-5-methyl-furan-2-carboxylic acidHCID 786859—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
ProductN-[4-(Biphenyl-4-yloxymethyl)-5-methyl-furan-2-carbonyl]-2-methyl-benzenesulphonamideHCID 1844463126.7%

Reaction Steps

A stirred solution of 4-(biphenyl-4-yloxymethyl)-5-methyl-furan-2-carboxylic acid (18) (50 mg, 0.162 mmoles), 2-methyl-benzenesulphonamide (42 mg, 0.243 mmoles) and 4-(N,N-dimethylamino)-pyridine (2.5 mg) in a mixture of tetrahydrofuran (8 ml) and acetonitrile (2 ml) was treated with 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (38 mg, 0.194 mmoles). The mixture was stirred at room temperature for 16 hours under an argon atmosphere. The reaction mixture was concentrated in vacuo and the residue was purified by HPLC to afford compound 60 (20 mg) as a white solid. LC/MS System D; Rt=11.09 mins, m/z (ES+)=462 (M+H for C26H23NO5S).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507754B2
Source datasetuspto-grants-2009_03
ORD IDord-560f3b6afd6544568b40a77d5eba2f20
Source noteuspto-grants-2009_03