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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28639Generated: October 28, 2026

Sodium Carbonate → 4-Chloro-6-(2,3,5-trichloro-phenyl)-pyrimidin-2-yl-amine-hydrochloride salt

https://huagongshe.com/reaction/28639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTriphenylphosphineHCID 11776—
Reactant2-Amino-4,6-dichloropyrimidineHCID 65522—
Reactant2,3,5-Trichlorophenylboronic acidHCID 5106508—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-Chloro-6-(2,3,5-trichloro-phenyl)-pyrimidin-2-yl-amine-hydrochloride saltHCID 8764664840.4%

Reaction Steps

A mixture of 2,3,5-trichloro-phenyl boronic acid (12 g, 53 mmol) and 4,6-dichloro-pyrimidin-2-yl-amine (10.5 g, 64 mmol) in ethylene glycol dimethyl ether (300 ml) under Argon atmosphere was stirred for 30 minutes. A mixture of palladium (II) acetate (1.8 g, 8 mmol), a solution of sodium carbonate (28.2 g, 270 mmol) in water (100 ml), and triphenylphosphine (4.2 g, 16 mmol) were added and the mixture was stirred for 18 hours. The mixture was treated with acetone (500 ml), filtered through a pad of celite under suction and concentrated under reduced pressure. The residue was treated with water (100 ml) and the mixture was stirred vigorously. The solid was filtered and dissolved in tetrahydrofuran (100 ml). Hydrogen chloride (4 M in dioxane, 20 ml) was added. After stirring for 1 hour, the solid was filtered and dried under reduced pressure. The solid was treated with ethyl acetate (50 ml) and stirred for 30 minutes. The solid was filtered and dried under reduced pressure to afford 4-chloro-6-(2,3,5-trichloro-phenyl)-pyrimidin-2-yl-amine-hydrochloride salt (3.7 g, 20% yield) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07419984B2
Source datasetuspto-grants-2008_09
ORD IDord-0925e98245224d7198554541457d5b6f
Source noteuspto-grants-2008_09