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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Diamino-6-chloropyrimidineHCID 67432—
ReactantMethyl 1H-imidazole-1-carboxylateHCID 580911—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-amino-6-chloro-4-pyrimidinecarbamateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04549019
Source datasetuspto-grants-1985_10
ORD IDord-1209f64a8f9f417f89431ae1108b4a1a
Source noteuspto-grants-1985_10