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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754396Generated: October 31, 2026

HCID 86704450, compound → HCID 86704452, compound

https://huagongshe.com/reaction/1754396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86704450HCID 86704450—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 86704452HCID 8670445289%

Reaction Steps

7-Azido-3,3-dimethylindolizin-5(1H)-one (0.3 g, 1.5 mmol) is dissolved in EtOH (20 ml). The clear solution is transferred to a Parr hydrogenation flask and placed under nitrogen. 10% Pd—C (0.25 g) was added to the Parr flask under nitrogen. The mixture was then transferred to a Pan hydrogenation apparatus, evacuated and filled with hydrogen (×3). The mixture was hydrogenated at 30 psi (optionally topping-up hydrogen) until LC/MS and TLC indicated complete reaction to the amine. After complete reaction, the mixture was placed under nitrogen and filtered through a small pad of Celite. The filter cake was washed with MeOH (×3) and the filtrate was concentrated under vacuum to leave the 7-amino-hexahydro-3,3-dimethylindolizin-5-(1H)-one in 89% yield (0.25 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169249B2
Source datasetuspto-grants-2015_10
ORD IDord-68019c724fae4c778928b9efface4d5a
Source noteuspto-grants-2015_10