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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043424Generated: November 2, 2026

Potassium Phosphate, Tribasic → (S)-N2-[1-(4-Fluorophenyl)ethyl]-N4-(pyrazin-2-yl)-6-(thiazol-5-yl)pyrimidine-2,4-diamine

https://huagongshe.com/reaction/2043424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantAminopyrazineHCID 78747—
Reactant(S)-4-chloro-N-[1-(4-fluorophenyl)ethyl]-6-(thiazol-5-yl)pyrimidine-2-amineHCID 86659392—
Solvent1,4-DioxaneHCID 31275—
Product(S)-N2-[1-(4-Fluorophenyl)ethyl]-N4-(pyrazin-2-yl)-6-(thiazol-5-yl)pyrimidine-2,4-diamineHCID 5683778757.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

To 155 mg of (S)-4-chloro-N-[1-(4-fluorophenyl)ethyl]-6-(thiazol-5-yl)pyrimidine-2-amine, 53 mg of 2-aminopyrazine, 72 mg of 4,5-bis(diphenylphosphino)-9,9′-dimethylxanthene, 196 mg of tripotassium phosphate and 81 mg of tris(dibenzylideneacetone)(chloroform)dipalladium, was added 4 ml of 1,4-dioxane, and the mixture was subjected to degassing, and substituted by argon gas, and then was stirred at 100° C. for 5 hours. The reaction solution was diluted with ethyl acetate. The solution was washed in turn with water and brine and then dried over magnesium sulfate. The solvent was distilled off under reduced pressure, and then the obtained residue was purified by silica gel column chromatography to obtain 105 mg of the objective compound as pale yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586591B2
Source datasetuspto-grants-2013_11
ORD IDord-764847ac57494c24a127b42c55087e86
Source noteuspto-grants-2013_11