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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 858049Generated: October 27, 2026

5,6-Diamino-1,3-dimethyluracil → HCID 58762837, compound

https://huagongshe.com/reaction/858049

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5,6-Diamino-1,3-dimethyluracilHCID 79501—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant2-(4-((Tert-butoxycarbonyl)amino)phenyl)acetic acidHCID 2824993—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
ProductHCID 58762837HCID 58762837—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of (4-tert-butoxycarbonylamino-phenyl)-acetic acid (0.825 mmol) and crude 5,6-diamino-1,3-dimethyl-1H-pyrimidine-2,4-dione (0.75 mmol) in N,N-dimethylformamide (3 mL) under argon at 25° C. was added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride(0.825 mmol) and 4-dimethylaminopyridine (0.15 mmol). The reaction was stirred at 25° C. for 18 h. At this time, the reaction was concentrated in vacuo. The residue was triturated with water and the resulting solid collected by filtration, washed well with water and dried in vacuo to afford crude {4-[(6-amino-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidin-5-ylcarbamoyl)-methyl]-phenyl}-carbamic acid tert-butyl ester as a light beige solid which was of sufficient purity for subsequent use without additional purification (87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07148229B2
Source datasetuspto-grants-2006_12
ORD IDord-11d19bd8e16c4b27b666cec2b11b9c65
Source noteuspto-grants-2006_12