HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892424Generated: October 28, 2026
Phthalimide → 2-(5,7-Difluoroquinolin-6-ylmethyl)isoindoline-1,3-dione
https://huagongshe.com/reaction/1892424
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phthalimide | HCID 6809 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | HCID 69810525 | HCID 69810525 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(5,7-Difluoroquinolin-6-ylmethyl)isoindoline-1,3-dione | HCID 69810340 | 81% |
Reaction Steps
A mixture of (E)-diisopropyl diazene-1,2-dicarboxylate (4.72 g, 23.36 mmol) and triphenylphosphine (6.13 g, 23.36 mmol) in THF (100 mL) was stirred for 15 min, and a solution of (5,7-difluoroquinolin-6-yl)methanol (3.80 g, 19.47 mmol) and isoindoline-1,3-dione (3.15 g, 21.42 mmol) in THF (200 mL) was added dropwise. The reaction mixture was heated at 40° C. for 24 h. After cooling and evaporating, the residue was purified by silica gel with hexane:EtOAc to provide 2-(5,7-difluoroquinolin-6-ylmethyl)isoindoline-1,3-dione (5.10 g, 81%). 1H-NMR (400 MHz, CDCl3) δ ppm 8.93 (m, 1H), 8.39 (m, 1H), 7.85 (m, 2H), 7.72 (m, 2H), 7.59 (d, 1H), 7.43 (m, 1H), 5.15 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08507676B2 |
|---|
| Source dataset | uspto-grants-2013_08 |
|---|
| ORD ID | ord-47d0ef24eff34bab92bd8250a958a934 |
|---|
| Source note | uspto-grants-2013_08 |
|---|