HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Acetate → 3-[(3-fluoro-6-methylphenanthridin-5(6H)-yl)carbonyl]phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 1-(2',4'-Difluoro-1,1'-biphenyl-2-yl)ethanone | HCID 22482272 | — |
| Reactant | 1-[2-(2,4-Difluorophenyl)phenyl]ethan-1-amine | HCID 22482376 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-[(3-fluoro-6-methylphenanthridin-5(6H)-yl)carbonyl]phenol | HCID 11500912 | — |
Reaction Steps
1-(-2′,4′-difluoro-biphenyl-2-yl)-ethylamine—The title compound was prepared from 1-(2′,4′-difluoro-1,1′-biphenyl-2-yl)ethanone (3.67 g, 15.8 mmol), anhydrous methanol (200 mL), ammonium acetate (12.2 g, 158 mmol), and sodium cyanoborohydride (1.99 g, 31.6 mmol) according to the procedure and in the same manner as described in Example 24, step b resulting in the isolation of a clear oil that was used without further purification. MS [(ES+), m/z]: 217 [M-16]+, benzylic cation as a result of the loss of NH2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07585871B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-1b36fa801b1d4d6c9ac0302aa85ce949 |
| Source note | uspto-grants-2009_09 |