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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827117Generated: November 1, 2026

6-Chloropurine → HCID 178525138, compound

https://huagongshe.com/reaction/1827117

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-ChloropurineHCID 5359277—
Reactant4-Aminomethyl-1-N-Cbz-piperidineHCID 21955499—
SolventDimethylformamideHCID 6228—
SolventSodium BicarbonateHCID 516892—
ProductHCID 178525138HCID 178525138—

Reaction Steps

In DMF (5 mL), benzyl 4-(aminomethyl)-1-piperidinecarboxylate (1.20 g, 4.83 mmol) and 6-chloropurine (448 mg, 2.49 mmol) were combined and treated with TEA in a single portion and aged under N2 at 100° C. for 18 h. The resulting reaction was diluted with sat. NaHCO3 and extracted with ethyl acetate (3×). The combined organics were washed with brine, dried over Na2SO4, filtered and concentrated in vacuo to give a brown oil which was purified by silica gel chromatography (20 g, 32–60 μm silica, 99:1:0.1 to 90:10:1 CH2Cl2:CH3OH:NH4OH) to give benzyl 4-[(9H-purin-6-ylamino)methyl]-1-piperidinecarboxylate as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053089B2
Source datasetuspto-grants-2006_05
ORD IDord-5fc47ceb49de47baa5ebe9e5beae7a9d
Source noteuspto-grants-2006_05