Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278997Generated: October 27, 2026

Pyrrolidine → 2-Benzyloxy-6-(pyrrolidin-1-yl)-benzo[de]isoquinoline-1,3-dione

https://huagongshe.com/reaction/278997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant2-Benzyloxy-6-bromo-benzo[de]isoquinoline-1,3-dioneHCID 22624038—
SolventWaterHCID 962—
Product2-Benzyloxy-6-(pyrrolidin-1-yl)-benzo[de]isoquinoline-1,3-dioneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362181B1
Source datasetuspto-grants-2002_03
ORD IDord-9b477e69511e4c228623e1033e7c1768
Source noteuspto-grants-2002_03