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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253836Generated: November 3, 2026

Ethyl 4-piperidinecarboxylate → HCID 59845591, compound

https://huagongshe.com/reaction/1253836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86600702HCID 86600702—
SolventWaterHCID 962—
ProductHCID 59845591HCID 5984559179.7%

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixture of the crude trifluoromethanesulfonic acid 1-(4-chloro-2,6-dimethylphenyl)-3,6-dimethyl-1H-pyrrolo[2,3-b]pyridin-4-yl ester (20.5 g), ethyl isonipecotate (74.4 g) and N,N-diisopropylethylamine (12.2 g) was heated at 150-170° C. for 1 hour. To the reaction mixture, water was added and extracted with ethyl acetate. The organic layer was washed with water, and brine, dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated under reduced pressure and the residue was purified by a silica gel column chromatography (silica gel: Wako Gel (C200), eluent: hexane/ethyl acetate=5:1) to give 1-[1-(4-chloro-2,6-dimethylphenyl)-3,6-dimethyl-1H-pyrrolo[2,3-b]pyridin-4-yl]piperidine-4-carboxylic acid ethyl ester (16.6 g) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455511B2
Source datasetuspto-grants-2013_06
ORD IDord-a6a41f1a13ad48b0a19945acae8e4b17
Source noteuspto-grants-2013_06