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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716859Generated: October 31, 2026

Purine → HCID 178420486, compound

https://huagongshe.com/reaction/716859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPurineHCID 1044—
ReactantAnilineHCID 6115—
ReactantPotassium CarbonateHCID 11430—
Reactant6-ChloropurineHCID 5359277—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178420486HCID 178420486—

Reaction Steps

The general procedure for the synthesis of purine derivatives is depicted in FIG. 1. The initial compound 6-chloropurine (1.0 eq.) was mixed with aniline (1.20 eq.) and K2CO3 (2.5 eq.) in 50.0 ml dioxane. The resultant mixture was charged in 100 mL round bottom flask with a stirring bar. The mixture was refluxed overnight and monitored by TLC. After the reaction finished, the solvent was removed and the remaining residue was extracted by ethyl acetate. After removing the solvent, the resultant crude product was purified by silica gel column chromatography eluting with CH2Cl2/MeOH (5%) to provide pure titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193711B2
Source datasetuspto-grants-2015_11
ORD IDord-f2e117a9e6a742a3af4dcf7ebec7395a
Source noteuspto-grants-2015_11