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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8593Generated: October 24, 2026

Diisopropylethylamine → 2-Phenyl-ethanesulfonic acid (6-chloro-5-p-tolyl-pyrimidin-4-yl)-amide

https://huagongshe.com/en/reaction/8593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4,6-Dichloro-5-(4-methylphenyl)pyrimidineHCID 21979554—
Reactant2-Phenyl-ethanesulfonic acid amide potassium saltHCID 68898150—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product2-Phenyl-ethanesulfonic acid (6-chloro-5-p-tolyl-pyrimidin-4-yl)-amideHCID 8659246959.6%

Reaction Conditions

Temperature5 °C

Reaction Steps

A solution of 2-phenyl-ethanesulfonic acid amide potassium salt (3.0 g), 4,6-dichloro-5-p-tolyl-pyrimidine (2.15 g) and Hunig's base (1.57 ml) in DMSO (50 ml) was stirred at rt for 20 h before it was diluted with water (500 ml) and extracted twice with diethyl ether (250 ml). The aqueous phase was acidified with acetic acid. The resulting suspension was cooled to 5° C. and filtered. The solid material was washed with water and diethyl ether, and dried at 40° C. under high vacuum to give 2-phenyl-ethanesulfonic acid (6-chloro-5-p-tolyl-pyrimidin-4-yl)-amide (2.08 g) as a grey powder. LC-MS: tR=5.23 min, [M+1]+=388.18, [M−1]−=386.14.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091201B2
Source datasetuspto-grants-2006_08
ORD IDord-de2c64610930487e978e7f18ba39fabb
Source noteuspto-grants-2006_08