HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079575Generated: November 2, 2026
Ethyl 4-piperidinecarboxylate → HCID 59845591, compound
https://huagongshe.com/reaction/2079575
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 4-piperidinecarboxylate | HCID 70770 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 86600702 | HCID 86600702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 59845591 | HCID 59845591 | 79.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07932259B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-5d3c4e7aebc441ebae2c3b4cc84309e1 |
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| Source note | uspto-grants-2011_04 |
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