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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067912Generated: November 1, 2026

Ethyl 4-piperidinecarboxylate → HCID 68726041, compound

https://huagongshe.com/reaction/2067912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
ReactantHCID 86660124HCID 86660124—
SolventDimethylformamideHCID 6228—
ProductHCID 68726041HCID 68726041—

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293757B2
Source datasetuspto-grants-2012_10
ORD IDord-1e5da6b067bb4cacbcff4f9b76c3f17b
Source noteuspto-grants-2012_10