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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264424Generated: November 1, 2026

Ethyl 4-amino-1-piperidinecarboxylate → Ethyl 4-[(4-methoxy-2-pyrimidinyl)amino]-1-piperidinecarboxylate

https://huagongshe.com/reaction/2264424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-amino-1-piperidinecarboxylateHCID 100867—
Reactant2-Chloro-4-methoxypyrimidineHCID 588935—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductEthyl 4-[(4-methoxy-2-pyrimidinyl)amino]-1-piperidinecarboxylateHCID 2423758042%

Reaction Steps

A mixture of 2-chloro-4-methoxy-pyrimidine (3.64 g, 25.21 mmol, 1.0 equiv; commercially available) and 4-amino-piperidine-1-carboxylic acid ethyl ester (4.34 g, 25.21 mmol, 1.0 equiv; commercially available) in anhydrous NMP (32 mL) was heated by microwave irradiation to 200° C. for 15 min. The organic phase was concentrated under reduced pressure and the residue extracted with ethyl acetate (3×50 mL) from a solution of 1 M NaOH (100 mL). The combined organic phases were dried over MgSO4 and the product purified with column chromatography on silica eluting with heptane/ethyl acetate (1:1) providing 2.93 g (42%) of the title compound. MS (ISP): 281.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855194B2
Source datasetuspto-grants-2010_12
ORD IDord-91c896b2649644249f4a01041a0ed3f9
Source noteuspto-grants-2010_12