HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-allyl-5-azaisatin → 1H-Pyrrolo[3,2-c]pyridine-2,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-allyl-5-azaisatin | HCID 19390720 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1H-Pyrrolo[3,2-c]pyridine-2,3-dione | HCID 10701965 | — |
Reaction Steps
A solution of N-allyl-5-azaisatin (5.3 mmol), (Ph3P)3RhCl (0.5 mmol) in aqueous toluene is stirred under a nitrogen atmosphere at room temperature overnight. The organic layer is dried (MgSO4) and the solvent is evaporated. The residue is stirred in 1N HCl/MeOH for 15 min after which time the methanol is evaporated and the pH of the water is adjusted to 7. A precipitate is formed and purified by silica gel chromatography (1% MeOH:CHCl3) to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05441955 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-13e4f4d258794ec5a2973b4328ee72fb |
| Source note | uspto-grants-1995_08 |