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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500768Generated: November 4, 2026

tert-butyl (3R)-3-aminopiperidine-1-carboxylate → HCID 86691786, compound

https://huagongshe.com/reaction/1500768

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl (3R)-3-aminopiperidine-1-carboxylateHCID 1501974—
ReactantHCID 86691787HCID 86691787—
SolventEthanolHCID 702—
ProductHCID 86691786HCID 8669178668%

Reaction Steps

A solution of 3-(4-chloropyrimidin-2-yl)pyrazolo[1,5-a]pyridine (Preparation 33, 130 mg, 0.56 mmol) and (R)-tert-butyl 3-aminopiperidine-1-carboxylate (326 mg, 1.63 mmol) in ethanol (5 mL) was heated overnight at 100° C. After cooling to ambient temperature, the solvent was evaporated under reduced pressure and the residue was taken up in a mixture of chloroform and water. The aqueous layer was separated and washed with chloroform (×2). The combined organic extracts were dried (MgSO4) and evaporated in vacuo. The crude product was purified by flash chromatography (dichloromethane to 95:5 dichloromethane/methanol) to give the title compound (150 mg, 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206183B2
Source datasetuspto-grants-2015_12
ORD IDord-952a0f7d3a2f4d72933ab6c2553550aa
Source noteuspto-grants-2015_12