HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165741Generated: October 26, 2026
Formaldehyde → 4,6-Dimethyl-2-(morpholin-4-ylthiocarbonylthiomethylamino)pyrimidine
https://huagongshe.com/reaction/2165741
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 2-Amino-4,6-dimethyl pyrimidine | HCID 13021 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4,6-Dimethyl-2-(morpholin-4-ylthiocarbonylthiomethylamino)pyrimidine | HCID 53998646 | — |
Reaction Steps
6.6 g (0.1 mole) of 85% potassium hydroxide and 8.9 g (0.1 mole) of morpholine are dissolved in 200 ml of water and, with cooling, 7.7 g (0.1 mole) of carbon disulfide are added. The mixture is stirred until a yellowish homogeneous solution is obtained. With cooling and stirring, 9.4 g (0.11 mole) of aqueous 35% formaldehyde and a solution of 12.7 g (0.1 mole) of 2-amino-4,6-dimethylpyrimidine and 9.7 g (0.1 mole) of methanesulfonic acid in 50 ml of water are added in succession. The reaction mixture is further stirred at room temperature, whereupon first an oil precipitates, which crystallises after a short time. After 24 hours the batch is diluted with 1 liter of water and the crystalline precipitate is filtered with suction and dried, affording 24 g (80% of theory) of the title compound with a melting point of 119°-121° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04940792 |
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| Source dataset | uspto-grants-1990_07 |
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| ORD ID | ord-bf3f2026785241afa0de28d55ec329c2 |
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| Source note | uspto-grants-1990_07 |
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