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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043423Generated: November 2, 2026

5-(Tributylstannyl)-1,3-thiazole → (S)-4-chloro-N-[1-(4-fluorophenyl)ethyl]-6-(thiazol-5-yl)pyrimidine-2-amine

https://huagongshe.com/reaction/2043423

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(Tributylstannyl)-1,3-thiazoleHCID 2763257—
Reactant(S)-4,6-Dichloro-N-[1-(4-fluorophenyl)ethyl]pyrimidin-2-amineHCID 86659372—
CatalystHCID 178418397HCID 178418397—
Product(S)-4-chloro-N-[1-(4-fluorophenyl)ethyl]-6-(thiazol-5-yl)pyrimidine-2-amineHCID 8665939252.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

286 mg of (S)-4,6-dichloro-N-[1-(4-fluorophenyl)ethyl]pyrimidine-2-amine (Reference Example 1), 411 mg of 5-(tributylstannyl)thiazole and 115 mg of tetrakis(triphenylphosphine)palladium were added in turn to degassed dimethylformamide, and then the mixture was stirred at 100° C. for 5 hours under argon atmosphere. 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 175 mg of (S)-4-chloro-N-[1-(4-fluorophenyl)ethyl]-6-(thiazol-5-yl)pyrimidine-2-amine as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586591B2
Source datasetuspto-grants-2013_11
ORD IDord-1d16acbe6c334646af8026091c4087f9
Source noteuspto-grants-2013_11