Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192549Generated: October 30, 2026

HCID 59226459, compound → HCID 59226506, compound

https://huagongshe.com/reaction/2192549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59226459HCID 59226459—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
ProductHCID 59226506HCID 5922650689%

Reaction Steps

A solution of 2-(5,5-dimethyl-3-(3-nitropyridin-4-yl)cyclohex-2-enyl)isoindoline-1,3-dione (1 eq) in acetic acid (0.1 M) was purged with nitrogen for 10 min. Then 10% Pd/C (0.10 eq) was added. The reaction mixture was stirred at room temperature overnight under an atmosphere of hydrogen. Solids were removed by filtration over celite, then rinsed with EtOAc and MeOH. The filtrate was concentrated, diluted with EtOAc and washed 2× with sat. aq. 2M Na2CO3. The organic layer was dried with MgSO4, filtered, and concentrated. The residue was purified by column (5% methanol in 1:1 ethyl acetate and hexanes) to give 2-(3-(3-aminopyridin-4-yl)-5,5-dimethylcyclohex-2-enyl)isoindoline-1,3-dione (89%). LC/MS (m/z): MH+=348.3, Rt=0.79.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329732B2
Source datasetuspto-grants-2012_12
ORD IDord-4d7ac1b0eb7e4940a379ec0d5ab0874a
Source noteuspto-grants-2012_12