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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046777Generated: November 1, 2026

HCID 59226459, compound → HCID 59226506, compound

https://huagongshe.com/reaction/2046777

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 numberUS08592455B2
Source datasetuspto-grants-2013_11
ORD IDord-d17cb62d0d1c4a13acd6184a1c542c0e
Source noteuspto-grants-2013_11