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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1099101Generated: October 30, 2026

Water → 5-Chloro-8-methoxy[1,2,4]triazolo[1,5-c]pyrimidin-2-amine

https://huagongshe.com/reaction/1099101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl [(2-chloro-5-methoxypyrimidin-4-yl)amino]carbonothioylcarbamateHCID 56949522—
CatalystSodium CarbonateHCID 10340—
SolventAcetonitrileHCID 6342—
Product5-Chloro-8-methoxy[1,2,4]triazolo[1,5-c]pyrimidin-2-amineHCID 5694957669.6%

Reaction Steps

Ethyl [(2-chloro-5-methoxypyrimidin-4-yl)amino]carbonothioylcarbamate (2) (290 mg, 1.0 mmol), hydroxylamine hydrochloride (143 mg, 2 eq), and sodium bicarbonate (170 mg, 2 eq) were combined. Water (5 mL) and acetonitrile (5 mL) were added at room temperature. The resulting slurry was stirred at room temperature overnight, then treated with 20 drops of saturated aqueous sodium carbonate solution. The resulting solution was sparged with nitrogen and cooled, producing the product as a chalky precipitate, which was collected by filtration (in two crops), washed with water, and dried to obtain the title compound as a solid (139 mg, 68%): mp 251° C.; 1H NMR (DMSO-d6) δ 7.73 (s, 1H), 3.98 (s 3H); 6.63 (s, 2H); 13C NMR (DMSO-d6): 166.30, 148.14, 128.91, 124.67, 57.51; Mass spec (accurate mass): Calcd for C6H6ClN5O 199.026087; found, 199.0256.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143395B2
Source datasetuspto-grants-2012_03
ORD IDord-4b0d709f73a241a9b8afc4f11907afef
Source noteuspto-grants-2012_03