HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247855Generated: November 3, 2026
Water → 2-[(3,5-dimethyl-4-methoxypyridin-2-yl)methyl]thio-6-methyl-4(3H)-pyrimidinone
https://huagongshe.com/reaction/2247855
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Methylthiouracil | HCID 667493 | — |
| Reactant | 2-(Chloromethyl)-4-methoxy-3,5-dimethylpyridin-1-ium chloride | HCID 45925697 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-[(3,5-dimethyl-4-methoxypyridin-2-yl)methyl]thio-6-methyl-4(3H)-pyrimidinone | HCID 135559185 | 36% |
Reaction Steps
After dissolving 0.22 g (4.0 mmol) of potassium hydroxide in the mixture of 15 ml of ethanol and 3 ml of water, first 0.28 g (2.0 mmol) of 6-methyl-2-thiouracil, then a solution of 0.44 g (2.0 mmol) of 2-chloromethyl-3,5-dimethyl-4-methoxypyridinium chloride (m.p.: 127°-128° C.) in 15 ml of ethanol are added. The reaction mixture is stirred at room temperature for 20 hours, then ethanol is evaporated under reduced pressure, 10 ml of water are added to the residue and the product is extracted 3 times with 5 ml of chloroform each. The combined organic phase is washed with water, dried over anhydrous magnesium sulfate and evaporated under reduced pressure. The residue is recrystallized from 2-propanol to obtain 0.21 g (36%) of the title compound as a white crystalline product, m.p.: 231°-233° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05037830 |
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| Source dataset | uspto-grants-1991_08 |
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| ORD ID | ord-48b8c66ff79d4cc18b4b20a622b10b48 |
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| Source note | uspto-grants-1991_08 |
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