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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460064Generated: October 29, 2026

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

https://huagongshe.com/reaction/460064

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 numberUS07196089B2
Source datasetuspto-grants-2007_03
ORD IDord-e636f6f4099a49b2a61507802024a8de
Source noteuspto-grants-2007_03