HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrrolidine → 2-Benzyloxy-6-(pyrrolidin-1-yl)-benzo[de]isoquinoline-1,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 2-Benzyloxy-6-bromo-benzo[de]isoquinoline-1,3-dione | HCID 22624038 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Benzyloxy-6-(pyrrolidin-1-yl)-benzo[de]isoquinoline-1,3-dione | HCID 22623998 | — |
Reaction Steps
Pyrrolidine (3 mL) was added to 2-benzyloxy-6-bromo-benzo[de]isoquinoline-1,3-dione (0.8 g, 2.1 mmol, from Example M) in the presence of DBU (0.05 mL). The mixture was refluxed for 2 hours and poured into water (50 mL). The precipitate formed was filtered and dried to give 0.8 g of 2-benzyloxy-6-(pyrrolidin-1-yl)-benzo[de]isoquinoline-1,3-dione. The hydrogenation of 2-benzyloxy-6-(pyrrolidin-1-yl)-benzo[de]isoquinoline-1,3-dione (0.4 g, 1.1 mmol) in the presence of 10% Pd/C (0.2 g) in DMA (30 mL) gave 0.27 g of the title compound, mp 268-270° C.;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06362181B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-9b477e69511e4c228623e1033e7c1768 |
| Source note | uspto-grants-2002_03 |