HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → HCID 58998504, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 58998396 | HCID 58998396 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58998504 | HCID 58998504 | 89% |
Reaction Steps
To a chilled suspension of 7-Fluoro-6-methoxy-2-(4-nitrophenyl)-2H-isoquinolin-1-one (3.14 g, 10 mmol) in dichloromethane (50 mL) was added neat boron tribromide (8 mL, 85 mmol) via syringe. The brown suspension was stirred at room temperature for 24 hr. The solvent was decanted, washed with cold DCM, leaving a black residue, which was triturated on ice with methanol (80 mL). The solid was collected by filtration, then washed with water and dried to give 2.66 g (89%) of 7-Fluoro-6-hydroxy-2-(4-nitro-phenyl)-2H-isoquinolin-1-one. RP-HPLC: 3.93 min; ES-MS (M+H)+=301.0; 1H-NMR (DMSO-d6) δ (ppm): 6.66 (d,1), 7.16 (d, 1), 7.43 (d, 1); 7.76 (d, 2), 7.84 (d, 1), 8.33 (d, 2), 11.1 (br s, 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07294635B2 |
| Source dataset | uspto-grants-2007_11 |
| ORD ID | ord-a7e22981418349d19aa8f4dd27058de7 |
| Source note | uspto-grants-2007_11 |