HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 1,3(2H,4H)-isoquinolinedione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | HCID 22503669 | HCID 22503669 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | 1,3(2H,4H)-isoquinolinedione | HCID 349435 | — |
Reaction Steps
3-Chloro-1-(4-ethylpiperazin-1-yl)isoquinoline (3.5 g) and 4-(1,3,2-dioxaborynan-2-yl)-1-(1,3-dioxolan-2-yl)benzene (5.0 g) were reacted in dimethylformamide (50 ml), in the presence of cesium carbonate (7.3 g) and tetrakistriphenylphosphinepalladium (0.3 g) at 80° C. in a nitrogen stream for 12 hr. The reaction solution was evaporated, and then partitioned between ethyl acetate and water. The resulting organic layer was washed with water, dried and evaporated. The resulting residue was purified by silica gel column chromatography (methylene chloride/methanol system), to give 4.66 g of the title compound as a pale yellow oil. (17-5) 1-(4-Ethylpiperazin-1-yl)-3-(4-formylphenyl)isoquinoline
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06875761B2 |
| Source dataset | uspto-grants-2005_04 |
| ORD ID | ord-03a85851618649aa8d5f7d5a82629d19 |
| Source note | uspto-grants-2005_04 |