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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190572Generated: November 1, 2026

Ethyl 4-piperidinecarboxylate → HCID 59318148, compound

https://huagongshe.com/reaction/2190572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 59318151HCID 59318151—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 59318148HCID 5931814855%

Reaction Conditions

Temperature95 °C

Reaction Steps

6-Chloro-N-(2-fluoro-4-iodo-phenyl)-nicotinamide (80 mg, 0.22 mmol) was dissolved in dioxane (6 mL) and the mixture was treated with diisopropyl ethyl amine (0.11 mL, 0.66 mmol), ethyl isonipecotate (100 mg, 0.66 mmol) and a catalytic amount of DMAP. This solution was then heated in a sealed tube at 95° C. for 21 h. The mixture was then cooled and the solvent was evaporated. The residue was chromatographed with a silica gel column and 20-40% EtOAc in hexanes gradient to afford the product. (60 mg, Yield: 55%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324385B2
Source datasetuspto-grants-2012_12
ORD IDord-ef639cbc6e7c409f81fd67d9f0341a44
Source noteuspto-grants-2012_12