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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036793Generated: November 1, 2026

Isopropyl 4-Hydroxypiperidine-1-carboxylate → HCID 86597364, compound

https://huagongshe.com/reaction/1036793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl 4-Hydroxypiperidine-1-carboxylateHCID 16745126—
Reactant4,6-Dichloro-5-ethylpyrimidineHCID 21828432—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86597364HCID 8659736440%

Reaction Steps

To a solution of 4,6-dichloro-5-ethyl-pyrimidine (1 g, 5.65 mmol) and 4-hydroxy-piperidine-1-carboxylic acid isopropyl ester (1.05 g, 5.65 mmol) in dry THF under nitrogen at 0° C., potassium tert-butoxide (1M solution in THF, 6.78 mL) was added dropwise. The reaction was stirred at rt for 30 min. The mixture was quenched with water and extracted with EtOAc (3×). The organic layer was washed with water, sat. NH4Cl and brine, followed by drying over sodium sulfate and concentration under vacuo. The resulting oil was purified by HPLC to afford 4-(6-chloro-5-ethyl-pyrimidin-4-yloxy)-piperidine-1-carboxylic acid isopropyl ester (0.74 g, 39.8%) as a colorless oil. Exact mass calculated for C15H22ClN3O3 327.13, found 328.2 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546429B2
Source datasetuspto-grants-2013_10
ORD IDord-e2789ecc7188474b801163ef269f9a81
Source noteuspto-grants-2013_10