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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050502Generated: October 27, 2026

Triphenylphosphine → (R)-tert-butyl 3-(isoquinolin-1-yloxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/1050502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactanttert-butyl (3S)-3-hydroxypiperidine-1-carboxylateHCID 1514399—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
ReactantHCID 178517620HCID 178517620—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product(R)-tert-butyl 3-(isoquinolin-1-yloxy)piperidine-1-carboxylateHCID 118114503—

Reaction Steps

A mixture of 1-hydroxyisoquinoline (1.00 g, 6.9 mmol), (S)-1-BOC-3-hydroxypiperidine (4.17 g, 20.7 mmol), Ph3P (7.23 g, 27.6 mmol) in THF (40 mL) was stirred at RT into a clear solution. DIAD (5.43 mL, 27.6 mmol) was added dropwise. The mixture was stirred at RT for 1 h and then at 50° C. for overnight. The mixture was diluted with EtOAc, washed with water ×3, dried, and concentrated in vacuo. The residue was subjected to flash column chromatography with 0% to 15% EtOAc in DCM to afford (R)-tert-butyl 3-(isoquinolin-1-yloxy)piperidine-1-carboxylate (53).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382246B2
Source datasetuspto-grants-2016_07
ORD IDord-44cedc3a07494322973daebb61f4e0eb
Source noteuspto-grants-2016_07