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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212815Generated: November 1, 2026

Acetic Anhydride → HCID 67414838, compound

https://huagongshe.com/reaction/2212815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant5H-Cyclopenta[b]pyridine-6,7-dione, 6-oximeHCID 85928843—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
ProductHCID 67414838HCID 67414838—

Reaction Steps

18 g (0.11 mol) of the compound of step c were dissolved in 500 ml of acetic acid and 500 ml of acetic acid anhydride and hydrogenated for 20 h at a pressure of 2 bar over 5 g of palladium on barium sulfate. The reaction mixture was filtered and evaporated. The residue was dissolved in 1000 ml of ethanol, treated with 10.8 ml of perchloric acid and hydrogenated for 10 h at 50° C. and a pressure of 3.5 bar over 5 g of palladium on charcoal (10%). The resulting mixture was evaporated, the residue taken up in dilute NaOH solution and extracted with ethyl acetate. Evaporation of the combined organic phases and subsequent chromatography of the residue yielded racemic N-(6,7-dihydro-5H-[1]pyrindin-6-yl)acetamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105513B2
Source datasetuspto-grants-2006_09
ORD IDord-c296e491c9d34ae4b96f9475c307af97
Source noteuspto-grants-2006_09