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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217890Generated: October 29, 2026

N-(2-Oxo-3-piperidyl)phthalimide → 2-(2-Methoxy-3-methyl-3,4,5,6-tetrahydropyridin-3-yl)-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/217890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-Oxo-3-piperidyl)phthalimideHCID 135339—
Reactant1H-Isoindole-1,3(2H)-dione, 2-(3-methyl-2-oxo-3-piperidinyl)-HCID 10445223—
Product2-(2-Methoxy-3-methyl-3,4,5,6-tetrahydropyridin-3-yl)-1H-isoindole-1,3(2H)-dioneHCID 67265465—

Reaction Steps

By analogy with the method described in example 1 (step 1.1), using 2-(3-methyl-2-oxopiperidin-3-yl)-1H-isoindole-1,3(2H)-dione (prepared by analogy to the method described in Liebigs Annalen der Chemie (1987), (7), 647-8. Archiv der Pharmazie (Weinheim, Germany) (1989), 322(8), 499-505, (Heterocycles (1996), 42(2), 537-42, Enantiomer (2001), 6(5), 275-279, Synthesis (1991), (5), 417-20)) in place of 3-phtalimidopiperidin-2-one, the compound was obtained as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198287B2
Source datasetuspto-grants-2012_06
ORD IDord-a0d2b4e073404b38b4263f344034a4ff
Source noteuspto-grants-2012_06