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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890974Generated: October 30, 2026

4-Chloro-6-(2-methoxyphenyl)pyrimidine → (3-[6-(2-methoxyphenyl)-4-pyrimidinyl]aminophenyl)-N-propylmethanesulfonamide

https://huagongshe.com/reaction/1890974

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-6-(2-methoxyphenyl)pyrimidineHCID 15206835—
Reactant(3-nitrophenyl)-N-propylmethanesulfonamideHCID 28636111—
SolventDimethylformamideHCID 6228—
Product(3-[6-(2-methoxyphenyl)-4-pyrimidinyl]aminophenyl)-N-propylmethanesulfonamideHCID 58550533—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of (3-nitrophenyl)-N-propylmethanesulfonamide (0.114 g, 0.5 mmol) and 4-chloro-6-(2-methoxyphenyl)-pyrimidine (0.110 g, 0.5 mmol) in DMFA (3 mL) was stirred at 80° C. till the end of the reaction (TLC control) and then concentrated under reduced pressure. The resulting residue was purified by column chromatography on silica to afford the (3-[6-(2-methoxyphenyl)-4-pyrimidinyl]aminophenyl)-N-propylmethanesulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507498B2
Source datasetuspto-grants-2013_08
ORD IDord-c0207984c9f64f9588eacb4dbf86e15e
Source noteuspto-grants-2013_08