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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452619Generated: November 1, 2026

tert-butyl (3S)-3-aminopiperidine-1-carboxylate → HCID 57526820, compound

https://huagongshe.com/reaction/1452619

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl (3S)-3-aminopiperidine-1-carboxylateHCID 1501975—
ReactantHCID 57526856HCID 57526856—
SolventAcetonitrileHCID 6342—
ProductHCID 57526820HCID 5752682022.9%

Reaction Conditions

Temperature85 °C

Reaction Steps

To an acetonitrile (5 mL) solution containing tert-butyl {6-[2-(tert-butyldimethylsilanyloxy)ethyl]-5-chloropyrazolo[1,5-a]pyrimidin-7-yl}[4-(2-methoxyethoxy)phenyl]carbamate (570 mg, 1.20 mmol), (S)-3-amino-1-tert-butoxycarbonylpiperidine (1.51 g) was added, and this mixture was stirred at 85° C. for 48 hr. The reaction solution was concentrated, and the residue was purified with column chromatography (35% ethyl acetate-hexane) to obtain the title compound (204 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07473694B2
Source datasetuspto-grants-2009_01
ORD IDord-ec18eaecbbeb46c3ba2a6c5675c32eb0
Source noteuspto-grants-2009_01