HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464774Generated: October 29, 2026
2,4-Diamino-6-chloropyrimidine → Methyl 2-amino-6-chloro-4-pyrimidinecarbamate
https://huagongshe.com/reaction/464774
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,4-Diamino-6-chloropyrimidine | HCID 67432 | — |
| Reactant | Methyl 1H-imidazole-1-carboxylate | HCID 580911 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 2-amino-6-chloro-4-pyrimidinecarbamate | HCID 13423619 | — |
Reaction Steps
46.3 g (0.32 mol) of 6-chloro-2,4-diamino-pyrimidine are dissolved in 1000 ml of tetrahydrofuran and treated with 57.9 g (0.517 mol) of potassium tert.butylate. The gel-like precipitate is stirred at room temperature for 1 hour. A solution of 60.5 g (0.48 mol) of 1-methoxycarbonylimidazole in 100 ml of ether is added thereto at a temperature of 10° within 90 minutes. The mixture is thereafter stirred at 25° for a further 2 hours, the solvent is then evaporated under reduced pressure and the residue is dissolved in ethyl acetate. The organic solution is washed with cold water and dried over sodium sulfate. After evaporation of the solvent under reduced pressure, the residue is crystallized from acetone/ether. After recrystallization from chloroform/methanol/hexane, there is obtained methyl 2-amino-6-chloro-4-pyrimidinecarbamate of melting point 225°-226°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04549019 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-1209f64a8f9f417f89431ae1108b4a1a |
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| Source note | uspto-grants-1985_10 |
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