Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | HCID 58998493 | HCID 58998493 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 69128203 | HCID 69128203 | 130% |
Reaction Steps
A 110 mg (0.28 mmol) portion of 5-Bromo-7-fluoro-6-methylamino-2-(4-nitro-phenyl)-2H-isoquinolin-1-one (Example 107) and 55 mg (2.2 equiv) of CuCN in 1.4 mL of NMP was heated to 200° C. for 2 h. After cooling to 50° C., 10 mL of 10% aq KCN was added, and mixture was stirred, filtered, washed with water and dried to give 123 mg (130%) of 7-Fluoro-6-methylamino-2-(4-nitro-phenyl)-1-oxo-1,2-dihydro-isoquinoline-5-carbonitrile. A 50 mg (0.15 mmol) portion of this 5-cyano material was reduced with 36 mg of Raney Nickel (Aldrich) in 1:1:2 water/AcOH/pyridine containing 58 mg of sodium hypophosphite. The reaction was then extracted 3 times with ethyl acetate, drying over Na2SO4 (anh.), and concentration in vacuo afforded 10 mg (20%) of the resulting aniline. This material was then coupled using the method described in Example 13 to give 7.8 mg (46%) of 5-chloro-N-[({4-[5-cyano-7-fluoro-6-(methylamino)-1-oxoisoquinolin-2(1H)-yl]phenyl}amino)carbonyl]thiophene-2-sulfonamide. ES-MS (M+H)+=532.1 (Cl).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07294635B2 |
|---|
| Source dataset | uspto-grants-2007_11 |
|---|
| ORD ID | ord-fbfa876953624e5690a635731fdfecf5 |
|---|
| Source note | uspto-grants-2007_11 |
|---|