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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091394Generated: November 1, 2026

Triethylamine → HCID 57877935, compound

https://huagongshe.com/reaction/1091394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Chloro-3-methyl-6-(3-fluoropyridin-4-yl)-3H-pyrimidin-4-oneHCID 59576812—
ReactantHCID 66594953HCID 66594953—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57877935HCID 5787793550%

Reaction Steps

A solution of (2S)-2-(4-(dimethylamino)phenyl)morpholine hydrochloride (0.20 g, 0.64 mmol), 2-chloro-1-methyl-6-oxo-4-(3-fluoropyridin-4-yl)-1,6-dihydropyrimidine (0.12 g, 0.53 mmol), and triethylamine (0.19 g, 1.92 mmol) in tetrahydrofuran (10 ml) was stirred at 95° C. for 3 hours. The solvent was evaporated off in vacuo and the residue treated with water and dichloromethane. The organic layer was dried over anhydrous sodium sulfate and the solvent was evaporated under reduced pressure. The obtained residue was purified by column chromatography on silica gel (chloroform-methanol, 10:1) to afford 2-((2S)-2-(4-(dimethylamino)phenyl)morpholin-4-yl)-6-(3-fluoropyridin-4-yl)-3-methyl-3H-pyrimidin-4-one (0.10 g, 50%) as yellow crystals

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129377B2
Source datasetuspto-grants-2012_03
ORD IDord-c816ff9c833c47eb8cbb272dc95cb257
Source noteuspto-grants-2012_03