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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648346Generated: October 27, 2026

Sodium hydride → 2-(2-Bromo-5-nitrophenyl)-4-[[2'-(N-t-butylsulfamoyl)-3-fluorobiphenyl-4-yl]methyl]-2,4-dihydro-5-ethyl-3H-1,2,4-triazol-3-one

https://huagongshe.com/reaction/1648346

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4'-(Bromomethyl)-N-t-butyl-3'-fluoro-2-biphenylsulfonamideHCID 10046521—
Reactant2-(2-Bromo-5-nitrophenyl)-2,4-dihydro-5-ethyl-3H-1,2,4-triazol-3-oneHCID 135503625—
SolventDimethylformamideHCID 6228—
Product2-(2-Bromo-5-nitrophenyl)-4-[[2'-(N-t-butylsulfamoyl)-3-fluorobiphenyl-4-yl]methyl]-2,4-dihydro-5-ethyl-3H-1,2,4-triazol-3-oneHCID 1007776788%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 2.00 g (6.39 mmol) of 2-(2-bromo-5-nitrophenyl)-2,4-dihydro -5-ethyl-3H-1,2,4-triazol-3-one (from Step B) and 184 mg (7.67 mmol) of sodium hydride in 7 mL of DMF was stirred at 50° C. for 3 hours. A solution of 4'-(bromomethyl)-N-t-butyl-3'-fluoro -2-biphenylsulfonamide (from Step F dissolved in 6 ml of DMF was then added and the resulting mixture was stirred at 50° C. for another 3 hours. The reaction mixture was quenched by addition of water followed by extractions with EtOAc, CH2Cl2, and MeOH. Water was removed and the organic layers were washed with brine, and dried over anhydrous Na2SO4. The entire crude product mixture thus obtained was flash chromatographed over silica gel (gradient elution using 0.5-2.0% MeOH in CH2Cl2) to afford 3.54 g (88%) of the title compound as a yellow solid (contaminated with some upper and lower Rf impurities by TLC but suitable for use in the next step without further purification), mp 223°-225° C.; mass spectrum (FAB) m/e 631, 633 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05436259
Source datasetuspto-grants-1995_07
ORD IDord-0738fe7d8b8141bb99396d26718be0ee
Source noteuspto-grants-1995_07