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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264429Generated: October 30, 2026

4-Amino-1-Boc-piperidine → HCID 68779241, compound

https://huagongshe.com/reaction/2264429

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
Reactant2-Chloro-4,6-dimethoxypyrimidineHCID 5152323—
SolventDimethylformamideHCID 6228—
ProductHCID 68779241HCID 68779241—

Reaction Steps

A mixture of 2-chloro-4,6-dimethoxy-pyrimidine (3.35 g, 19.19 mmol, 1.0 equiv; commercially available) and 4-amino-piperidine-1-carboxylic acid tert-butyl ester (5.0 g, 24.94 mmol, 1.3 equiv; commercially available) in anhydrous DMF (100 mL) was heated to 100° C. for 48 h. 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 by silica column chromatography using a MPLC system (CombiFlash Companion, Isco Inc.) eluting with a gradient of heptane/ethyl acetate providing 1.97 g (30%) of the title compound. MS (ISP): 339.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855194B2
Source datasetuspto-grants-2010_12
ORD IDord-10cd4f85ff914db9baa0d113ac221015
Source noteuspto-grants-2010_12