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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181228Generated: October 25, 2026

Diisopropylethylamine → 4-Methyl-phenyl sulfamic acid-[6-chloro-5-(p-tolyl)-4-pyrimidinyl]-amide

https://huagongshe.com/reaction/1181228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4,6-Dichloro-5-(4-methylphenyl)pyrimidineHCID 21979554—
Reactant4-Methyl-phenyl sulfamic acid amide potassium saltHCID 69512930—
SolventDimethyl SulfoxideHCID 679—
SolventMethanolHCID 887—
Product4-Methyl-phenyl sulfamic acid-[6-chloro-5-(p-tolyl)-4-pyrimidinyl]-amideHCID 2197955262.1%

Reaction Steps

To 4,6-dichloro-5-p-tolyl-pyrimidine (Referential Example 7) (2.0 g) dissolved in DMSO (35 ml) was added di-isopropyl-ethyl-amine (1.46 ml) followed by addition of 4-methyl-phenyl sulfamic acid amide potassium salt (2.78 g) [prepared from the product described in Referential Example 19 and potassium tert.-butylate in methanol followed by evaporation of the solvent]. The mixture was stirred for 48 h at rt then poured onto water (500 ml) and diethylether (250 ml) was added and the solution was stirred for 30 min. The layers were separated and the water layer was acidified with acetic acid (2.0 ml) and cooled to 0° C. for 1 h. The precipitated product was filtered off and washed with water and diethylether and dried to give 4-methyl-phenyl sulfamic acid-[6-chloro-5-(p-tolyl)-4-pyrimidinyl]-amide (2.02 g). tR=5.00 min (LC); [M+H]+=389.11 (ES+);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07285549B2
Source datasetuspto-grants-2007_10
ORD IDord-e4cd05bddae34722a19c60dae901e047
Source noteuspto-grants-2007_10