Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505839Generated: October 30, 2026

Hydrochloric Acid → 5-Amino-3H-thiazolo[4,5]pyrimidine-2-one

https://huagongshe.com/reaction/505839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantCarbamide PeroxideHCID 31294—
Reactant5-Aminothiazolo[4,5-d]pyrimidine-2(3H)-thioneHCID 57756068—
SolventWaterHCID 962—
Product5-Amino-3H-thiazolo[4,5]pyrimidine-2-oneHCID 2476403967%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of NaOH (0.6 g, 15 mmol, 3 eq) in water (20 ml) was added 5-amino-3H-thiazolo[4,5-d]pyrimidin-2-thione (0.92 g, 5 mmol, 1.0 eq). The mixture was stirred to dissolve. Urea hydrogen peroxide (2.8 g, 30 mmol, 6 eq) was slowly added dropwise to the above solution, keeping the temperature below 50° C. The reaction was then cooled down to room temperature (about 25° C.). Concentrated HCl (37%, 6 ml) was added to the above solution until the pH is less than 1. The mixture is stirred at room temperature for 30 minutes. Celite (2 g) was added to the solution and the solution was filtered and washed with water (10 ml). To the filtrate was added 50% NaOH solution to adjust the pH to 5-5.5. The solution was heated up to 50-60° C. for 30 minutes. The resulting solution was cooled down to room temperature, filtered, and washed with water, dried at 50° C. under vacuum to give 0.56 g (67%) of 5-amino-3H-thiazolo[4,5-d]pyrimidin-2-one as a pale yellow solid. 1H NMR, HPLC and LCMS analyses of this product are identical to the product described from Procedure A in Step 2 of Example 1 above.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781581B2
Source datasetuspto-grants-2010_08
ORD IDord-6dffb2525dea4ebea8fa558bc0e2b5ac
Source noteuspto-grants-2010_08