HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067912Generated: November 1, 2026
Ethyl 4-piperidinecarboxylate → HCID 68726041, compound
https://huagongshe.com/reaction/2067912
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 4-piperidinecarboxylate | HCID 70770 | — |
| Reactant | HCID 86660124 | HCID 86660124 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 68726041 | HCID 68726041 | — |
Reaction Steps
5-(5-(4-(Difluoromethoxy)phenyl)pyrimidin-2-ylamino)-2-methylphenethyl methanesulfonate 51b (0.9 mmol), ethyl piperidine-4-carboxylate (2.2 mmol) are dissolved in DMF (10 mL) and heated to 90° C. for 4 h then cooled to rt. The reaction mixture is partitioned with EtOAc and water. The organic layer is washed with water, brine, dried over magnesium sulfate, filtered and reduced to dryness. The crude material is purified by column chromatography on silica with hexane:EtOAc=1:1 to 100% EtOAc as eluant to yield ethyl 1-(5-(5-(4-(difluoromethoxy)phenyl)pyrimidin-2-ylamino)-2-methylphenethyl)piperidine-4-carboxylate 52 as clear viscous oil. MS (m/z) (M+1)+: 511.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08293757B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-1e5da6b067bb4cacbcff4f9b76c3f17b |
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| Source note | uspto-grants-2012_10 |
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