HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1981508Generated: October 28, 2026
Benzyl Chloride → 1-Benzyl-3-bromo-5-(pyrimidin-4-yl)pyridin-2(1H)-one
https://huagongshe.com/reaction/1981508
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 3-Bromo-5-(pyrimidin-4-yl)pyridin-2(1H)-one | HCID 13276678 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Benzyl-3-bromo-5-(pyrimidin-4-yl)pyridin-2(1H)-one | HCID 13645097 | — |
Reaction Steps
A solution of sodium methoxide (1.85 g) in 100 ml DMF and 30 ml MeOH is added to a stirred, suspension of 3-bromo-5-(4-pyrimidinyl)-2(1H)-pyridone in 100 ml DMF. Benzyl chloride (3.9 ml) is added to the reaction mixture, and the mixture is heated to 70° C. for 2 hours and allowed to cool to RT overnight. The reaction mixture is filtered and the solvent evaporated in vacuo. The residue is suspended in H2O, filtered and dried. The resultant solid is dissolved in hot isopropanol, filtered through charcoal and recrystallized, yielding 1-benzyl-3-bromo-5-(4-pyrimidinyl)-2-pyridone, M.P. 189°-191.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04593028 |
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| Source dataset | uspto-grants-1986_06 |
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| ORD ID | ord-1eb83b3cdefa42a4971f091ecd8d150d |
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| Source note | uspto-grants-1986_06 |
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