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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8613Generated: October 27, 2026

Citric Acid → 2-Thiophen-2-yl-ethanesulfonic acid [5-(4-chloro-phenyl)-6-(2-hydroxy-ethoxy)-pyrimidin-4-yl]-amide

https://huagongshe.com/reaction/8613

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
Reactant2-Thiophen-2-yl-ethanesulfonic acid [6-chloro-5-(4-chloro-phenyl)-pyrimidin-4-yl]-amideHCID 86592473—
SolventEthylene GlycolHCID 174—
SolventWaterHCID 962—
Product2-Thiophen-2-yl-ethanesulfonic acid [5-(4-chloro-phenyl)-6-(2-hydroxy-ethoxy)-pyrimidin-4-yl]-amideHCID 23548250—

Reaction Conditions

Temperature110 °C

Reaction Steps

2-Thiophen-2-yl-ethanesulfonic acid [6-chloro-5-(4-chloro-phenyl)-pyrimidin-4-yl]-amide (930 mg) was added to a solution of K-tert. butylate (1.16 g) in ethylene glycol (10 ml). The mixture was stirred at 110° C. for 12 h before it was diluted with water (150 ml), acidified with 10% aq. citric acid (13 ml). The resulting precipitate was collected, washed with water and diethyl ether and dried to give (820 mg) 2-thiophen-2-yl-ethanesulfonic acid [5-(4-chloro-phenyl)-6-(2-hydroxy-ethoxy) -pyrimidin-4-yl]-amide as a beige powder. LC-MS: tR=4.43 min, [M+1]+=440.01, [M−1]−=437.99.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091201B2
Source datasetuspto-grants-2006_08
ORD IDord-8a743ff8858e40c99c6d6143fe72b8cd
Source noteuspto-grants-2006_08