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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241768Generated: November 1, 2026

Methyl iodide → HCID 58114936, compound

https://huagongshe.com/reaction/241768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantIsobutyric acid 7-(2-chloro-4-methyl-thiazol-5-yl)-6-oxo-5,6-dihydro-pyrido[2,3-b]pyrazin-8-yl esterHCID 58114926—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 58114936HCID 58114936—

Reaction Steps

Isobutyric acid 7-(2-chloro-4-methyl-thiazol-5-yl)-6-oxo-5,6-dihydro-pyrido[2,3-b]pyrazin-8-yl ester (Example 2.4) (0.10 g), methyl iodide (0.18 ml) and potassium carbonate (0.075 g) were heated in acetonitrile (4 ml) in a microwave to 100° C. for 10 minutes. The reaction mixture was allowed to cool to ambient temperature and then diluted with ethyl acetate and water. The phases were separated and the organic phase was washed with water, aqueous sodium hydrogen carbonate (saturated) and brine, dried over magnesium sulfate and concentrated to give Compound No. B2 of Table B (0.078 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653078B2
Source datasetuspto-grants-2014_02
ORD IDord-d231bd5d87734108a45614a913a2dfae
Source noteuspto-grants-2014_02