HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900691Generated: October 31, 2026
Ethyl 4-piperidinecarboxylate → HCID 23117199, compound
https://huagongshe.com/reaction/900691
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 4-piperidinecarboxylate | HCID 70770 | — |
| Reactant | HCID 23117206 | HCID 23117206 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23117199 | HCID 23117199 | — |
Reaction Steps
1.3 ml of ethyl isonipecotate was added to a 5 ml THF solution of 413 mg of 5,6-dichloro-N-[4-(4-chlorothiophen-2-yl)-5-(piperidin-1-ylmethyl)-1,3-thiazol-2-yl]nicotinamide, and the mixture was stirred for 5 days. After the solvent was distilled off under reduced pressure, a saturated sodium hydrogencarbonate aqueous solution was added, and the resulting precipitate was collected by filtration. The precipitate was dissolved in chloroform, and a saturated sodium hydrogencarbonate aqueous solution was added. The mixture was extracted with chloroform, and dried over magnesium sulfate. The solvent was distilled off under reduced pressure, and the resulting residue was purified by silica gel column chromatography using hexane:EtOAc (4:1 to 3:1) as an elution solvent to obtain 468 mg of ethyl 1-(3-chloro-5-{[4-(4-chlorothiophen-2-yl)-5-(piperidinomethyl)thiazol-2-yl]carbamoyl}-2-pyridyl)piperidine-4-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07361658B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-f38df0b3102f47a196448104e1347c74 |
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| Source note | uspto-grants-2008_04 |
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