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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | Ethyl 1-benzyl-3-oxopiperidine-4-carboxylate hydrochloride | HCID 2723880 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 7-Benzyl-5,6,7,8-tetrahydro-2-(methylthio)pyrido[3,4-d]pyrimidin-4(4aH)-one | HCID 69222301 | 88% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07414131B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-e1a897dc1efb467da5c04e4508ca5457 |
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| Source note | uspto-grants-2008_08 |
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