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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192546Generated: November 1, 2026

HCID 59226503, compound → HCID 59226443, compound

https://huagongshe.com/reaction/2192546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59226503HCID 59226503—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
ProductHCID 59226443HCID 5922644373%

Reaction Steps

To a solution of 2-(3-(3-nitropyridin-4-yl)cyclohex-2-enyl)isoindoline-1,3-dione (1.0 equiv.) in acetic acid (0.1 M) was added 10% Pd/C (0.2 equiv.) and the reaction was stirred under a H2 balloon. After 3 days, the reaction was filtered through Celite, washed with ethyl acetate and methanol, the filtrate was diluted with ethyl acetate and washed twice with sat. 2M Na2CO3. The organic phase was dried with magnesium sulfate, filtered and concentrated. The crude material was triturated with hexanes and ethyl acetate to afford 2-(3-(3-aminopyridin-4-yl)cyclohexyl)isoindoline-1,3-dione in 73% yield. LC/MS=322.2 (M+H), Rt=0.64 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329732B2
Source datasetuspto-grants-2012_12
ORD IDord-0eb693b1ce974f5da5207b097c303a2b
Source noteuspto-grants-2012_12