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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510054Generated: October 25, 2026

Ethyl 6-amino-2-chloro-5-nitropyrimidine-4-carboxylate → HCID 66614187, compound

https://huagongshe.com/reaction/510054

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 6-amino-2-chloro-5-nitropyrimidine-4-carboxylateHCID 4390083—
ReactantHexabutyldistannaneHCID 6327815—
Reactant5-Fluoro-1-(2-fluorobenzyl)-3-iodo-1H-pyrazolo[3,4-b]pyridineHCID 58065602—
CatalystHCID 178418476HCID 178418476—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 66614187HCID 66614187—

Reaction Conditions

Temperature100 °C

Reaction Steps

Under argon, 3.85 g (10.91 mmol) of the compound from example 24A were initially charged in dioxane (100 ml) and the reaction mixture was purged with argon. Subsequently, 8.27 ml (16.36 mmol) of hexabutylditin and 2.96 g (12.00 mmol) of ethyl 6-amino-2-chloro-5-nitropyrimidine-4-carboxylate (prepared according to J. Chem. Res. 1989, 2086-2097) were added. Thereafter, 3.83 g (5.45 mmol) of bis(triphenylphosphine)palladium(II) chloride were added and the reaction mixture was stirred at 100° C. overnight. Thereafter, the mixture was cooled to RT and filtered through Celite, and the residue was washed with methanol. The filtrate was concentrated, and the residue was extracted by stirring with ethyl acetate and filtered off. The filtrate was concentrated and the residue was purified by means of prep. HPLC (eluent: acetonitrile/water with 0.1% formic acid gradient). This gave 1.36 g (71% purity, 14% of theory) of crude product, which was converted without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096592B2
Source datasetuspto-grants-2015_08
ORD IDord-60ec768fa4434d84970c61afd5162e51
Source noteuspto-grants-2015_08