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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890984Generated: October 30, 2026

4-Chloro-6-(2-methoxyphenyl)pyrimidine → C-{3-[6-(2-methoxy-phenyl)-pyrimidin-4-ylamino]-phenyl}-N-(3-methoxy-propyl)-methanesulfonamide

https://huagongshe.com/reaction/1890984

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-6-(2-methoxyphenyl)pyrimidineHCID 15206835—
ReactantC-(3-amino-phenyl)-N-(3-methoxy-propyl)-methanesulfonamideHCID 43256757—
SolventDimethylformamideHCID 6228—
ProductC-{3-[6-(2-methoxy-phenyl)-pyrimidin-4-ylamino]-phenyl}-N-(3-methoxy-propyl)-methanesulfonamideHCID 59840905—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of C-(3-amino-phenyl)-N-(3-methoxy-propyl)-methanesulfonamide (0.129 g, 0.50 mmol) and 4-chloro-6-(2-methoxyphenyl)-pyrimidine (0.110 g, 0.10 mmol) in DMFA (3 mL) was stirred at 80° C. till the reaction completion (TLC control), then evaporated in vacuo. The resulting residue was purified by column chromatography on silica gel yielding C-{3-[6-(2-methoxy-phenyl)-pyrimidin-4-ylamino]-phenyl}-N-(3-methoxy-propyl)-methanesulfonamide

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507498B2
Source datasetuspto-grants-2013_08
ORD IDord-6b7cb39ae9a04729be4695fc76840799
Source noteuspto-grants-2013_08