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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207808Generated: November 1, 2026

HCID 58547762, compound → HCID 58547782, compound

https://huagongshe.com/reaction/2207808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 58547762HCID 58547762—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanolHCID 702—
ProductHCID 58547782HCID 5854778276.5%

Reaction Steps

To a N2 purged round bottom flask was added benzyl 3-(3-(3,6-dihydro-2H-pyran-4-yl)pyrazin-2-yloxy)azetidine-1-carboxylate (see PREPARATION P28.2; 490 mg, 1.334 mmol), pearlman's catalyst (37.5 mg, 0.267 mmol) and EtOH (10 mL). A balloon of H2 was placed atop the round bottom flask. After 20 hours, the reaction was filtered through CELITE® and the cake was washed with EtOAc. The filtrate was concentrated in vacuo to give 2-(azetidin-3-yloxy)-3-(tetrahydro-2H-pyran-4-yl)pyrazine (240 mg, 1.020 mmol, 76% yield), as a tan residue. MS (ESI) m/z 236.1 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376450B2
Source datasetuspto-grants-2016_06
ORD IDord-e56aa6631aba46fda4e8b91ea4ee527d
Source noteuspto-grants-2016_06