HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982091Generated: October 31, 2026
Hydrochloric Acid → Methyl (4,6-dimethoxypyrimidin-2-yl)carbamate
https://huagongshe.com/reaction/1982091
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Dimethyl Carbonate | HCID 12021 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Amino-4,6-dimethoxypyrimidine | HCID 118946 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl (4,6-dimethoxypyrimidin-2-yl)carbamate | HCID 13314628 | 70.2% |
Reaction Steps
2-Amino-4,6-dimethoxypyrimidine (56 g) was added portionwise to 50% sodium hydride (42.8 g) in 1000 ml of dry tetrahydrofuran. After stirring for 0.5 hour, dimethylcarbonate (58.5 g) was added dropwise with cooling. The mixture was stirred under nitrogen for about 16 hours at ambient temperature. Concentrated HCl (80 ml) was added slowly as external cooling was used to maintain a pot temperature of about 25° C. Saturated aqueous sodium chloride (80 ml) was then added. The solvents were decanted from the precipitated solids and dried over sodium sulfate. Filtration and evaporation of the solvents afforded the crude material which was recrystallized from hexane to yield 54 g of the title compound, m.p. 81°-83° C. The IR spectrum showed characteristic absorption bands at 3400 and 1760 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04595407 |
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| Source dataset | uspto-grants-1986_06 |
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| ORD ID | ord-1fc401e8b5ae4220ae3426d1069bc814 |
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| Source note | uspto-grants-1986_06 |
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