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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198671Generated: October 31, 2026

Benzenesulfonyl chloride → HCID 10349512, compound

https://huagongshe.com/reaction/1198671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
Reactant5-n-Butyl-2,4-dihydro-4-[(2'-sulfamoylbiphenyl-4-yl)methyl]-2-[2-(trifluoromethyl)phenyl]-3H-1,2,4-triazol-3-oneHCID 10346902—
ProductHCID 10349512HCID 10349512—

Reaction Conditions

Temperature60 °C

Reaction Steps

The title compound was prepared from 5-n-butyl-2,4-dihydro-4-[(2'-sulfamoylbiphenyl-4-yl)methyl]-2-[2-(trifluoromethyl)phenyl]-3H-1,2,4-triazol-3-one (from Example 13, Step C) according to the procedure of Example 14, except that a total of 2.4 equivalents of benzenesulfonyl chloride was used, and the mixture was heated at 60° C. for 4 hours. The crude produce was purified by flash chromotography on silica gel (gradient elution with 0.5-5% MeOH in CH2Cl2). The residue from evaporation of the product fractions was partitioned between CH2Cl2 and 1N HCl. The organic phase was dried (Na2SO4), filtered, and concentrated in vacuo to give the title compound as a cream-colored, sticky solid, homogeneous by TLC in 9:1 CH2Cl2 --MeOH; mass spectrum (FAB) m/e 671 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05281614
Source datasetuspto-grants-1994_01
ORD IDord-b7248b4d65be49e1bfbf94e7885f2a5a
Source noteuspto-grants-1994_01