Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5146Generated: October 28, 2026

1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → Oxanosine

https://huagongshe.com/reaction/5146

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant[(amino)carbonyl]amino-1-(beta-D-ribofuranosyl)-1H-imidazole-4-carboxylic acidHCID 131718114—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductOxanosineHCID 477547—

Reaction Steps

1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (78 mg, 0.41 mmol) was added to a solution of 5-[[(amino)carbonyl]amino-1-(β-D-ribofuranosyl)-1H-imidazole-4-carboxylic acid (19 mg, 0.063 mmol) in water (2 mL) and CH3OH (5 mL) and the mixture was stirred at room temperature overnight. The reaction was quenched by addition of excess 60% aqueous acetic acid. After 30 minutes, the mixture was diluted with water, concentrated to remove CH3OH and lyophilized. The resulting powder (100 mg) was chromatographed on reverse phase silica gel [10 g, flash, stepwise gradient elution: water (200 mL), 10% CH3OH in water (v/v, 100 mL), 20% CH3OH in water (v/v, 100 mL), 10-mL fractions]. Fractions containing the product were combined, concentrated under reduced pressure and lyophilized to give oxanosine: 16 mg (89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05243042
Source datasetuspto-grants-1993_09
ORD IDord-b09968f7a78948329b0580e276d90a67
Source noteuspto-grants-1993_09