HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(2-Oxo-3-piperidyl)phthalimide → 2-(2-Methoxy-3-methyl-3,4,5,6-tetrahydropyridin-3-yl)-1H-isoindole-1,3(2H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(2-Oxo-3-piperidyl)phthalimide | HCID 135339 | — |
| Reactant | 1H-Isoindole-1,3(2H)-dione, 2-(3-methyl-2-oxo-3-piperidinyl)- | HCID 10445223 | — |
| Product | 2-(2-Methoxy-3-methyl-3,4,5,6-tetrahydropyridin-3-yl)-1H-isoindole-1,3(2H)-dione | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08198287B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-a0d2b4e073404b38b4263f344034a4ff |
| Source note | uspto-grants-2012_06 |