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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279389Generated: October 31, 2026

Sodium Methoxide → 5,8-Dimethoxy-[1,2,4]triazolo[1,5-c]pyrimidin-2-amine

https://huagongshe.com/reaction/279389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
Reactant3-Amino-5,8-dimethoxy[1,2,4]triazolo[4,3-c]pyrimidineHCID 22624874—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product5,8-Dimethoxy-[1,2,4]triazolo[1,5-c]pyrimidin-2-amineHCID 1144688892.9%

Reaction Steps

3-Amino-5,8-dimethoxy[1,2,4]triazolo[4,3-c]-pyrimidine (9.762 g, 0.050 mole) was loaded into a 500 mL three necked flask equipped with an overhead stirrer, condenser, addition funnel, and thermocouple temperature probe. Methanol (70 mL) was added and the mixture was stirred to form a slurry. Sodium methoxide (16.716 g of a 25% solution in methanol) was added dropwise over 28 min, after which the mixture was stirred at room temperature for 3 h. The reaction mixture was then diluted with water (135 mL) and stirred for an additional 1.5 h. The product solids were recovered by filtration through Whatman #54 paper using a Buchner funnel and aspirator vacuum. After washing with water, the solids were dried in vacuo at room temperature to give 9.064 g of 2-amino-5,8-dimethoxy[1,2,4]triazolo[1,5-c]pyrimidine (yield=92.8%): 1H NMR (300 MHz, DMSO-d6) 3.88 (s, 3H), 4.04 (s, 3H), 6.38 (br s, 2H), 7.48 (s, 1H); MS(GC, 70eV) 195 (M+, 85%), 194 (100%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362335B1
Source datasetuspto-grants-2002_03
ORD IDord-c8e82912bac14f63b05611cbfce069e2
Source noteuspto-grants-2002_03