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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198694Generated: October 26, 2026

4'-(Bromomethyl)-N-t-butyl-3'-fluoro-2-biphenylsulfonamide → 2-(2-Bromo-5-nitrophenyl)-4-[[2'-(N-t-butylsulfamoyl)-3-fluorobiphenyl-4-yl]methyl]-5-n-butyl-2,4-dihydro-3H-1,2,4-triazol-3-one

https://huagongshe.com/reaction/1198694

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4'-(Bromomethyl)-N-t-butyl-3'-fluoro-2-biphenylsulfonamideHCID 10046521—
Reactant2-(2-Bromo-5-nitrophenyl)-5-n-butyl-2,4-dihydro-3H-1,2,4-triazol-3-oneHCID 135720080—
Product2-(2-Bromo-5-nitrophenyl)-4-[[2'-(N-t-butylsulfamoyl)-3-fluorobiphenyl-4-yl]methyl]-5-n-butyl-2,4-dihydro-3H-1,2,4-triazol-3-oneHCID 1034940593%

Reaction Steps

The alkylation of 2-(2-bromo-5-nitrophenyl)-5-n-butyl-2,4-dihydro-3H-1,2,4-triazol-3-one (from Example 30, Step A) with [3-fluoro-2'-(N-t-butylsulfamoyl)-biphenyl-4-yl]methyl bromide (from Step B) was carried out according to the procedure of Example 8, Step A, to give a 93% yield of the title compound as a stiff, brownish foam, mp 137°-139° C., homogeneous by TLC in 98:2 CH2Cl2 --MeOH; mass spectrum (FAB) m/e 666, 668 (M+Li)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05281614
Source datasetuspto-grants-1994_01
ORD IDord-f5b1568060854c3eb224c8bfe4b8d97c
Source noteuspto-grants-1994_01