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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601066Generated: October 26, 2026

Bromine → 4-[5-Amino-1-(6-phenoxy-benzothiazol-2-yl)-1H-[1,2,4]triazol-3-ylamino]-benzenesulfonamide

https://huagongshe.com/reaction/601066

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant5-Amino-3-(4-sulfamoyl-phenylamino)-[1,2,4]triazole-1-carbothioic acid (4-phenoxy-phenyl)-amideHCID 58976467—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
Product4-[5-Amino-1-(6-phenoxy-benzothiazol-2-yl)-1H-[1,2,4]triazol-3-ylamino]-benzenesulfonamideHCID 589764117%

Reaction Steps

Bromine (7 μl, 1 equivalent) was added to a stirred suspension of 5-amino-3-(4-sulfamoyl-phenylamino)-[1,2,4]triazole-1-carbothioic acid (4-phenoxy-phenyl)-amide in dichloromethane (3 ml). The reaction mixture was stirred at room temperature for 18 hours. A solution of bromine (7 μl) in acetic acid (1 ml) was then added to push the reaction to completion: the reaction mixture was stirred for a further four hours. A white solid precipitated and was removed by filtration to afford the title compound (5 mg; 7% yield). 1H NMR (400 MHz, DMSO-d6) 7.05-7.20 (8H, m), 7.35-7.50 (4H, m), 7.70-7.75 (2H, d), 7.80-7.85 (2H, d), 9.90-9.95 (1H, s); MS (ES+) m/e=480

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902239B2
Source datasetuspto-grants-2011_03
ORD IDord-9045ec227c094215a061a223c921cdf4
Source noteuspto-grants-2011_03