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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2219949Generated: October 31, 2026

Methyl iodide → 7-Benzyl-5,6,7,8-tetrahydro-2-(methylthio)pyrido[3,4-d]pyrimidin-4(4aH)-one

https://huagongshe.com/reaction/2219949

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantThioureaHCID 2723790—
ReactantEthyl 1-benzyl-3-oxopiperidine-4-carboxylate hydrochlorideHCID 2723880—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
Product7-Benzyl-5,6,7,8-tetrahydro-2-(methylthio)pyrido[3,4-d]pyrimidin-4(4aH)-oneHCID 6922230188%

Reaction Conditions

Temperature100 °C

Reaction Steps

The suspension of ethyl N-benzyl-3-oxo-4-piperidine-carboxylate hydrochloride (8.9 g, 30 mmol) and thiourea (4.56 g, 60 mmol) in the solution of sodium methoxide in methanol (34 mL, 25% wt) was stirred at 100° C. in a sealed tube overnight. Iodomethane (5.1 g, 42 mmol) was added dropwise to the reaction mixture after cooled to room temperature and stirred at room temperature for 1 hr. Solvent was removed in vacuo and residue was dissolved in water (100 mL) and was extracted by CHCl3 and i-PrOH (3:1, 10×40 mL), dried over sodium sulfate. Solvent was removed in vacuo, product was obtained as a beige powder (7.6 g, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07414131B2
Source datasetuspto-grants-2008_08
ORD IDord-e1a897dc1efb467da5c04e4508ca5457
Source noteuspto-grants-2008_08