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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475324Generated: October 29, 2026

Sodium Chloride → 8-isopropyl-5-methyl-2-methylsulphanyl-8H-pyrido[2,3-d]pyrimidin-7-one

https://huagongshe.com/reaction/475324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantSodium hydrideHCID 24758—
Reactant1,4-DioxaneHCID 31275—
Reactant1-(4-Isopropylamino-2-methylsulphanyl-pyrimidin-5-yl)-ethanoneHCID 57461138—
Product8-isopropyl-5-methyl-2-methylsulphanyl-8H-pyrido[2,3-d]pyrimidin-7-oneHCID 11436613—

Reaction Conditions

Temperature20 °C

Reaction Steps

Sodium hydride (16.75 g, 0.042 mol) is placed in 200 mL dioxane and combined with triethylphosphonoacetate (83.8 mL, 0.419 mmol), so that the temperature does not exceed 5° C. After the addition is complete, the mixture is heated to 20° C. and 1-(4-isopropylamino-2-methylsulphanyl-pyrimidin-5-yl)-ethanone (11.1 g, 0.049 mol) dissolved in 100 mL dioxane is added thereto. The mixture is stirred for 16 h at 90° C., then combined with 10% sodium chloride solution and extracted with ethyl acetate. The organic phase is dried, the solvent is eliminated in vacuo and the crude product is purified by normal phase chromatography (cyclohexane/ethyl acetate 90:10→50:50 in 45 min; flow 200 mL/min) and 8-isopropyl-5-methyl-2-methylsulphanyl-8H-pyrido[2,3-d]pyrimidin-7-one (HPLC-MS: tRet.=1.74 min; MS(M+H)+=250; method FECS1) is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637549B2
Source datasetuspto-grants-2014_01
ORD IDord-cf67001d168a4aea86c70ac4ca3f66b9
Source noteuspto-grants-2014_01