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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8602Generated: October 25, 2026

4,6-Dichloro-5-(2-methoxyphenoxy)-2-(pyridin-4-YL)pyrimidine → 2-Phenyl-ethanesulfonic acid [6-chloro-5-(2-methoxy-phenoxy)-2-pyridin-4-yl-pyrimidin-4-yl]-amide

https://huagongshe.com/reaction/8602

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,6-Dichloro-5-(2-methoxyphenoxy)-2-(pyridin-4-YL)pyrimidineHCID 11175458—
Reactant2-Phenyl-ethanesulfonic acid amide potassium saltHCID 68898150—
SolventDimethylformamideHCID 6228—
Product2-Phenyl-ethanesulfonic acid [6-chloro-5-(2-methoxy-phenoxy)-2-pyridin-4-yl-pyrimidin-4-yl]-amideHCID 8659247178.1%

Reaction Steps

A solution of 4,6-dichloro-5-(2-methoxyphenoxy)-2-(4-pyridyl)-pyrimidine (2 g) and 2-phenyl-ethanesulfonic acid amide potassium salt (2.82 g, Referential Example 1e) in DMF (50 ml) was stirred at rt for 16 h. Bulk of the solvent was evaporated before it was diluted with diethyl ether (50 ml). The mixture was acidified with 10% aq. citric acid. The precipitate that formed was collected, washed with diethyl ether (100 ml) and dried to give 2-phenyl-ethanesulfonic acid [6-chloro-5-(2-methoxy-phenoxy)-2-pyridin-4-yl-pyrimidin-4-yl]-amide (2.23 g) as a beige powder. LC-MS: tR=4.93 min, [M+1]+=497.22, [M−1]−=494.96.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091201B2
Source datasetuspto-grants-2006_08
ORD IDord-50ab374672784712afdda58eb7ef9ef4
Source noteuspto-grants-2006_08