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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067900Generated: November 1, 2026

Ethyl 4-piperidinecarboxylate → HCID 68728956, compound

https://huagongshe.com/reaction/2067900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
ReactantHCID 86660120HCID 86660120—
SolventDimethylformamideHCID 6228—
ProductHCID 68728956HCID 68728956—

Reaction Conditions

Temperature95 °C

Reaction Steps

2-(3-(5-(4-(Difluoromethoxy)phenyl)pyrimidin-2-ylamino)phenoxy)ethyl methanesulfonate 40b (0.4 mmol), ethyl piperidine-4-carboxylate (0.9 mmol) are dissolved in DMF (3 mL) and heated to 95° C. for 6 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 product is triturated with MeOH and filtered to yield ethyl 1-(2-(3-(5-(4-(difluoromethoxy)phenyl)pyrimidin-2-ylamino)phenoxy)ethyl)piperidine-4-carboxylate 41 as white solid. MS (m/z) (M+1)+: 513.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293757B2
Source datasetuspto-grants-2012_10
ORD IDord-b7943aac52694a1987bd9a08e200c5d7
Source noteuspto-grants-2012_10