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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440890Generated: October 25, 2026

5-Nitroso-2,4,6-pyrimidinetriamine → 2,4,7-Triamino-6-(2-chlorophenyl)pteridine

https://huagongshe.com/reaction/440890

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Nitroso-2,4,6-pyrimidinetriamineHCID 70504—
Reactant(o-Chlorophenyl)acetonitrileHCID 76112—
ReactantSodium MethoxideHCID 10942334—
SolventDimethylformamideHCID 6228—
Product2,4,7-Triamino-6-(2-chlorophenyl)pteridineHCID 15278935—

Reaction Steps

A stirred solution of 1.5 grams (0.010 mole) of 2,4,6-triamino-5-nitrosopyrimidine in 80 mL of N,N-dimethylformamide was heated to reflux, and 2.0 grams (0.01 3 mole) of 2-chlorophenylacetonitrile was added in one portion. Upon completion of addition, the reaction mixture was cooled, and 0.7 gram (0.013 mole) of sodium methoxide was added in one portion. The reaction mixture was again heated at reflux for 15 minutes. The reaction mixture was cooled in an ice-bath and then was filtered to collect a solid. The solid was slurried in diethyl ether and then was again collected by filtration, yielding, when dried, 2.5 grams of 2,4,7-triamino-6-(2-chlorophenyl)pteridine. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521190
Source datasetuspto-grants-1996_05
ORD IDord-026491380cda4feb8509110ad50d91ee
Source noteuspto-grants-1996_05