HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247848Generated: November 2, 2026
Methylthiouracil → 4(1H)-Pyrimidinone, 2-(((2-(dimethylamino)phenyl)methyl)thio)-6-methyl-
https://huagongshe.com/reaction/2247848
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylthiouracil | HCID 667493 | — |
| Reactant | Thiouracil | HCID 1269845 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 178486212 | HCID 178486212 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Sodium ethoxide | HCID 2723922 | — |
| Product | 4(1H)-Pyrimidinone, 2-(((2-(dimethylamino)phenyl)methyl)thio)-6-methyl- | HCID 135744258 | 47.7% |
Reaction Steps
355 mg (2.5 mmol) of 6-methyl-2-thiouracil are dissolved in a sodium ethoxide solution prepared from 116 mg (5.05 mmol) of sodium metal and 15 ml of anhydrous ethanol. The mixture is gently warmed to dissolve the thiouracil, then 515 mg (2.5 mmol) of (2-chloromethylphenyl)-dimethylammonium chloride are added and the reaction mixture is refluxed under stirring for 1 hour. Sodium chloride is immediately precipitated from the solution. After evaporation under reduced pressure the residue is taken up in water, extracted 3 times with 20 ml of chloroform each, then the combined organic phase is washed with 20 ml of water, dried over anhydrous magnesium sulfate and evaporated under reduced pressure. The pale yellow oily residue is rubbed with an 1:1 mixture of benzene and petroleum ether to obtain 287 mg (47.7%) of the title compound as a white crystalline product, m.p.: 151°-153° 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-baa6d9552ea542a68ccfd12b5de6b346 |
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| Source note | uspto-grants-1991_08 |
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