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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464122Generated: October 30, 2026

2-Amino-4,6-dimethyl pyrimidine → N-(2-Chlorobenzene-1-sulfonyl)-N'-(4,6-dimethylpyrimidin-2-yl)carbamimidic acid

https://huagongshe.com/reaction/464122

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4,6-dimethyl pyrimidineHCID 13021—
Reactant2-Chlorobenzenesulfonyl chlorideHCID 76187—
ReactantPotassium cyanateHCID 11378442—
SolventAcetonitrileHCID 6342—
ProductN-(2-Chlorobenzene-1-sulfonyl)-N'-(4,6-dimethylpyrimidin-2-yl)carbamimidic acidHCID 182458—

Reaction Steps

A slurry of 23.8 g (0.10 mole) 2-chlorobenzenesulfonyl chloride, 16.2 g (0.2 mole) potassium cyanate, 15.5 g (0.11 moles) 4,6-dimethyl-2-pyrimidinamine in 150 ml acetonitrile was stirred at reflux for 5 hours. The reaction was cooled to 25° and filtered. The solids were dissolved in water, filtered, and the filtrate acidified to give a solid A. The reaction filtrate was distilled in vacuo to remove solvent. The residue and Solid A were combined, dissolved in 200 ml of 5% sodium hydroxide and extracted with methylene chloride. The aqueous layer was then acidified, the solids collected, washed with water and dried to give 18.9 g (50.6% of theory) of the title compound. The m.p. and IR spectrum of the title compound were identical to those of an authentic sample prepared as described in U.S. Pat. No. 4,169,719.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04546179
Source datasetuspto-grants-1985_10
ORD IDord-45525a606d9a4dfda4be3b9345eb677f
Source noteuspto-grants-1985_10