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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2252721Generated: October 25, 2026

Ethylene Glycol → Ethanesulfonic acid [6-(2-hydroxy-ethoxy)-5-p-tolyl-pyrimidin-4-yl]-amide

https://huagongshe.com/reaction/2252721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantEthanesulfonic acid (6-chloro-5-p-tolyl-pyrimidin-4-yl)-amideHCID 59645274—
ProductEthanesulfonic acid [6-(2-hydroxy-ethoxy)-5-p-tolyl-pyrimidin-4-yl]-amideHCID 59645277—

Reaction Conditions

Temperature100 °C

Reaction Steps

Ethanesulfonic acid (6-chloro-5-p-tolyl-pyrimidin-4-yl)-amide (363 mg) was added to a solution of potassium tert.-butoxide (427 mg) in ethylene glycol (7 ml) and stirred at 100° C. for 7 days. The reaction mixture was then poured onto ice/water and extracted with ethyl acetate. The crude product was purified by chromatography over silicagel with DCM/MeOH=9/1 to give ethanesulfonic acid [6-(2-hydroxy-ethoxy)-5-p-tolyl-pyrimidin-4-yl]-amide (310 mg) as a white powder. LC-MS: tR: 3.47, [M+H]+: 338.13.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07323465B2
Source datasetuspto-grants-2008_01
ORD IDord-1eec02ef45494ea5958f5f53f6737d22
Source noteuspto-grants-2008_01