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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79099Generated: October 26, 2026

Cyanuric chloride → 4-tert-butyl-N-methyl-N-(3-(aminosulfonyl)phenyl)benzamide

https://huagongshe.com/reaction/79099

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanuric chlorideHCID 7954—
ReactantTriethylamineHCID 8471—
ReactantAmmonium HydroxideHCID 14923—
Reactant3-(4-tert-butyl-N-methylbenzamido)benzenesulfonic acidHCID 58988055—
SolventAcetoneHCID 180—
Product4-tert-butyl-N-methyl-N-(3-(aminosulfonyl)phenyl)benzamideHCID 24855318—

Reaction Conditions

Temperature120 °C

Reaction Steps

A solution of 3-(4-tert-butyl-N-methylbenzamido)benzenesulfonic acid (12 mg, 35 μmol), cyanuric chloride (7.0 mg, 40 μmol), and triethylamine (6.0 μL, 40 μmol) in acetone (0.5 mL) was sealed in a glass tube and heated in a microwave oven at 120° C. for 10 min. Concentrated ammonium hydroxide (150 μL) was added, and the reaction was stirred for 6 h. The reaction was filtered, and the filtrate was purified by preparative reverse phase HPLC using 10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA) to give 4-tert-butyl-N-methyl-N-(3-(aminosulfonyl)phenyl)benzamide. LC/MS: m/z 347.3 (M+H)+ at 2.86 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841483B2
Source datasetuspto-grants-2014_09
ORD IDord-0cf14ec331364fe0a309edd917005dbb
Source noteuspto-grants-2014_09