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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378356Generated: October 31, 2026

Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) → N-(5-chloro-3-methoxypyrazin-2-yl)-4'-hydroxy-N-(isobutoxycarbonyl)-2-biphenylsulphonamide

https://huagongshe.com/reaction/1378356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
ReactantHCID 53756881HCID 53756881—
SolventEthanolHCID 702—
ProductN-(5-chloro-3-methoxypyrazin-2-yl)-4'-hydroxy-N-(isobutoxycarbonyl)-2-biphenylsulphonamideHCID 2291129197.8%

Reaction Steps

N-(5-Chloro-3-methoxypyrazin-2-yl)- N-(isobutoxycarbonyl)-4'-[2-(2 H)-tetrahydropyranyloxy]-2-biphenylsulphonamide (1.15 g) and pyridinium-p-toluenesulphonate (50 mg) in ethanol (50 ml) was heated at 60° C. for 3 hours. Volatile material was removed by evaporation and the residue was triturated with etherexane (1:1 v/v) to give N-(5-chloro-3-methoxypyrazin-2-yl)-4'-hydroxy- N-(isobutoxycarbonyl)-2-biphenylsulphonamide (0.96 g), m.p. 175°-177° C.; microanalysis found: C, 53.9; H, 4.8; N, 8.2%; C21H22C1N3O6 requires: C, 53.7; H, 4.5; N, 8.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05668137
Source datasetuspto-grants-1997_09
ORD IDord-2a231f1f8cee4e5bb2d0d4d0d041e51e
Source noteuspto-grants-1997_09