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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064347Generated: October 30, 2026

Chlorosuccinimide → 2-Amino-4-(1,2-dimethylimidazol-5-yl)-5-chloropyrimidine

https://huagongshe.com/reaction/1064347

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
Reactant2-Amino-4-(1,2-dimethylimidazol-5-yl)pyrimidineHCID 22273509—
SolventAcetic AcidHCID 176—
Product2-Amino-4-(1,2-dimethylimidazol-5-yl)-5-chloropyrimidineHCID 22273560233%

Reaction Conditions

Temperature65 °C

Reaction Steps

2-Amino-4-(1,2-dimethylimidazol-5-yl)pyrimidine (Method 26; 378 mg, 2 mmol) and N-chlorosuccimide (267 mg, 2 mmol) were dissolved in glacial acetic acid (7 ml) under an atmosphere of nitrogen. The reaction mixture was heated at 65° C. for 18 hours when further N-chlorosuccinimide (89 mg, 0.66 mmol) was added and the reaction heated at 65° C. for an additional 2 hours. The volatiles were removed by evaporation and the residue dissolved in water (10 ml). The solution was adjusted to pH 11-12 by addition of 40% aqueous sodium hydroxide solution. The precipitated solid was collected by filtration and washed sparingly with water, dried under vacuum at 60° C. to give the title compound (344 mg, 77%) as a yellow solid. NMR 2.35 (s, 3H, 3.75 (s, 3H), 4.83 (s, 2H), 7.53 (s, 1H), 8.27 (s, 1H); m/z 224.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06969714B2
Source datasetuspto-grants-2005_11
ORD IDord-acab7ec0e0684739985ff5a03ff4bc82
Source noteuspto-grants-2005_11