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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198688Generated: October 25, 2026

[2'-(N-t-Butylsulfamoyl)biphenyl-4-yl]methyl bromide → 2-(2-Bromo-5-nitrophenyl)-4-[[2'-(N-t-butylsulfamoyl)biphenyl-4-yl]methyl]-5-n-butyl-2,4-dihydro-3H-1,2,4-triazol-3-one

https://huagongshe.com/reaction/1198688

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[2'-(N-t-Butylsulfamoyl)biphenyl-4-yl]methyl bromideHCID 15282100—
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)biphenyl-4-yl]methyl]-5-n-butyl-2,4-dihydro-3H-1,2,4-triazol-3-oneHCID 1007791792%

Reaction Steps

The alkylation of 2-(2-bromo-5-nitrophenyl)-5-n-butyl-2,4-dihydro-3H-1,2,4-triazol-3-one (from Step A) with [2'-(N-t-butylsulfamoyl)biphenyl-4-yl]methyl bromide (from Example 7) was carried out according to the procedure of Example 8, Step A, to give a 92% yield of the title compound as a yellow solid, mp 126°-128° C.; homogeneous by TLC in 98:2 CH2Cl2 --MeOH; mass spectrum (FAB) m/e 642, 644 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05281614
Source datasetuspto-grants-1994_01
ORD IDord-d629c9888b564344abbb34e62ef5d050
Source noteuspto-grants-1994_01