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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1099207Generated: October 31, 2026

HCID 66811607, compound → HCID 66811231, compound

https://huagongshe.com/reaction/1099207

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66811607HCID 66811607—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 66811231HCID 66811231100%

Reaction Steps

To a solution of tert-butyl 2-(5-{1-[(benzyloxy)carbonyl]azetidin-3-yl}-1,3,4-oxadiazol-2-yl)-3-phenylpiperidine-1-carboxylate (200 mg, 0.39 mmol) in ethanol (10 ml) was added 10% palladium on carbon (20.0 mg). The reaction was charged with 1 atm hydrogen gas and allowed to stir for 1 h. The reaction was filtered through celite, and the filtrate was concentrated to yield tert-butyl 2-(5-azetidin-3-yl-1,3,4-oxadiazol-2-yl)-3-phenylpiperidine-1-carboxylate (100%). LCMS (M+H)=385.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143405B2
Source datasetuspto-grants-2012_03
ORD IDord-743bb96fd0004f53b472622e235dcd65
Source noteuspto-grants-2012_03