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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354842Generated: November 2, 2026

Ethyl 4-piperidinecarboxylate → HCID 178450378, compound

https://huagongshe.com/reaction/2354842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
ReactantHCID 10292152HCID 10292152—
SolventEthanolHCID 702—
ProductHCID 178450378HCID 17845037844%

Reaction Steps

2-Butoxy-9-(6-chloro-3-pyridylmethyl)-8-methoxyadenine (0.28 mg, 0.77 mmol) was added to 4-ethoxycarbonylpiperidine (10 ml), and the mixture was refluxed under stirring for 8 hours. After the mixture was allowed to cool, ethanol was added thereto. The resulting solid was filtered and purified by column chromatography (SiO2 20 g, eluting solvent: CHCl3/MeOH=80/1˜20/1) to give the captioned compound (0.15 g, 1.41 mmol, yield: 44%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754728B2
Source datasetuspto-grants-2010_07
ORD IDord-14f1d4a64f7a49ffb4470cfeb53e93d3
Source noteuspto-grants-2010_07