HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phthalic Anhydride → 2-(2-(2-Oxo-1,2-dihydropyridin-4-yl)ethyl)isoindoline-1,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-(2-aminoethyl)pyridin-2(1H)-one hydrobromide | HCID 68379399 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 2-(2-(2-Oxo-1,2-dihydropyridin-4-yl)ethyl)isoindoline-1,3-dione | HCID 68379255 | 76% |
Reaction Conditions
| Temperature | 140 °C |
|---|
Reaction Steps
A mixture of 4-(2-aminoethyl)pyridin-2(1H)-one hydrobromide (400 mg, 1.83 mmol), isobenzofuran-1,3-dione (271 mg, 1.83 mmol) and DIEA (472 mg, 3.66 mmol) in 30 mL of xylene was stirred at 140° C. for 6 hours. The solvent was removed under reduce pressure. The residue was purified by silica gel chromatography, eluting with DCM/MeOH (30/1) to give 2-(2-(2-oxo-1,2-dihydropyridin-4-yl)ethyl)isoindoline-1,3-dione (370 mg, 76%) as a white sold. LC-MS: 269 [M+H]+, tR=1.23 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08921383B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-d8e7b8022f5342a5b911bd180d829a1c |
| Source note | uspto-grants-2014_12 |