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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426277Generated: November 2, 2026

Toluene → 2-Chloro-5-(2-ethoxy-vinyl)-pyrimidin-4-ylamine

https://huagongshe.com/reaction/2426277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant4-Amino-5-bromo-2-chloropyrimidineHCID 2763293—
Reactant(Z)-1-Ethoxy-2-(tributylstannyl)etheneHCID 2763294—
CatalystHCID 178418397HCID 178418397—
SolventEthyl AcetateHCID 8857—
Product2-Chloro-5-(2-ethoxy-vinyl)-pyrimidin-4-ylamineHCID 5734897346%

Reaction Conditions

Temperature110 °C

Reaction Steps

A 500 mL round bottomed flask is charged with 5-bromo-2-chloropyrimidin-4-ylamine (1) (10 g, 48 mmol), tetrakis(triphenylphosphine)palladium(0) (2.8g, 2.5 mmol), and toluene (200 mL). Tributyl-(2-ethoxyvinyl)-stannane (22 g, 60 mmol) is added and the reaction heated to 110° C. with stirring for approximately 15 hours. After cooling to room temperature, the solution is diluted with 100 mL ethyl acetate and washed with water and brine. The organic extract is dried over Na2SO4, filtered, and concentrated under reduced pressure. Purification by column chromatography (SiO2, Hexane:Ethyl acetate/5:1) provides 2 (4.4 g, 46%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968557B2
Source datasetuspto-grants-2011_06
ORD IDord-fd9622c534054b589b3de758a0ec4964
Source noteuspto-grants-2011_06