Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029387Generated: November 1, 2026

Hydrochloric Acid → Hydrochloric Acid

https://huagongshe.com/reaction/1029387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAmmonium HydroxideHCID 14923—
ReactantSodium DithioniteHCID 24489—
ReactantHCID 86745618HCID 86745618—
Reactant2-(2-Amino-5-nitro-6-oxo-3,6-dihydropyrimidin-4-yl)-3-(thiophen-3-yl)propanenitrileHCID 135980345—
SolventSodium HydroxideHCID 14798—
ProductHydrochloric AcidHCID 313—
Product2,6-Diamino-3,5-dihydro-7-(3-thienylmethyl)-4H-pyrrolo(3,2-d)pyrimidin-4-oneHCID 135418361—

Reaction Conditions

Temperature90 °C

Reaction Steps

2,6-Diamino-3,5™dihydro-7-(3-thienylmethyl)-4H-pyrrolo-[3,2-d]pyrimidin-4-one. To a solution of 2-Amino-1,6-dihydro-5-nitro-6-oxo-α-(3-thienylmethyl)-4-pyrimidineacetonitrile prepared above (5.0 g) in 1N NaOH (300 mL) is added sodium dithionite (20 g). The reaction mixture is heated for 30 min at 90° C. and then is acidified (pH 1) with conc HCl while still hot. The reaction mixture is cooled and neutralized with ammonium hydroxide. The resulting precipitate is collected by filtration, washed with cold water and dried under vacuum. The crude product is added to 100 mL conc HCl in small portions with stirring and the hydrochloride salt is collected by filtration. The product is recrystallized from 1N HCl to give 2,6-Diamino-3,5-dihydro-7-(3-thienylmethyl)-4H-pyrrolo [3,2-d]pyrimidin4-one as the monohydro-chloride salt (2.35 g), mp>185° C. (dec). ##STR19##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05102879
Source datasetuspto-grants-1992_04
ORD IDord-1f079b75175244739425dbb3fd3eaa41
Source noteuspto-grants-1992_04