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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356087Generated: November 1, 2026

Tributyl(2,3-dihydrofuran-5-yl)stannane → 2-Amino-4-(4,5-dihydro-furan-2-yl)-6-methylsulfanyl-pyrimidine-5-carbonitrile

https://huagongshe.com/reaction/1356087

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyl(2,3-dihydrofuran-5-yl)stannaneHCID 14323397—
Reactant2-Amino-4-bromo-6-methylsulfanyl-pyrimidine-5-carbonitrileHCID 18753230—
CatalystHCID 178418476HCID 178418476—
Solvent1,4-DioxaneHCID 31275—
Product2-Amino-4-(4,5-dihydro-furan-2-yl)-6-methylsulfanyl-pyrimidine-5-carbonitrileHCID 1850763649%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirred solution of 700 mg (2.86 mmol) 2-amino-4-bromo-6-methylsulfanyl-pyrimidine-5-carbonitrile in 25 ml dry dioxane under argon at room temperature were added 1.13 g (3.14 mmol) tributyl-(4,5-dihydro-furan-2-yl)-stannane and 281 mg (0.40 mmol) bis(triphenylphosphine)palladium(II) chloride. The reaction mixture was heated at 100° C. for 18 h, then cooled to room temperature and concentrated in vacuo. Flash chromatography (ethyl acetate/hexane 1/1) afforded 325 mg (49%) 2-amino-4-(4,5-dihydro-furan-2-yl)-6-methylsulfanyl-pyrimidine-5-carbonitrile as a yellow crystalline solid. ES-MS m/e (%): 257 (M+Na+, 47), 235 (M+H+, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586441B2
Source datasetuspto-grants-2003_07
ORD IDord-61088bec13a24ffc975fe7cb8f17ddd8
Source noteuspto-grants-2003_07