HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 4-Cyanomethyl-8-fluoro-3-oxo-3,4-dihydro-2H-quinoxaline-1-carboxylic acid 2-methyl-4-(2,3,4,5-tetrahydrobenzo[b]azepine-1-carbonyl)benzylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (4-(Aminomethyl)-3-methylphenyl)(2,3,4,5-tetrahydro-1H-benzo[b]azepin-1-yl)methanone | HCID 15896086 | — |
| Reactant | (5-Fluoro-2-oxo-3,4-dihydro-2H-quinoxalin-1-yl)acetonitrile | HCID 23111114 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Cyanomethyl-8-fluoro-3-oxo-3,4-dihydro-2H-quinoxaline-1-carboxylic acid 2-methyl-4-(2,3,4,5-tetrahydrobenzo[b]azepine-1-carbonyl)benzylamide | HCID 11584492 | — |
Reaction Steps
To a solution of (5-fluoro-2-oxo-3,4-dihydro-2H-quinoxalin-1-yl)acetonitrile from Example 13A (183 mg, 0.89 mmol) in THF (2 ml) were added a solution of phosgene in toluene (20%, 0.61 ml, 1.2 mmol) and diisopropylethylamine (200 μl, 1.2 mmol). The mixture was stirred for 2 h. To the mixture were added a solution of (4-aminomethyl-3-methylphenyl)-(2,3,4,5-tetrahydrobenzo[b]azepin-1-yl)methanone from Example F (260 mg, 0.89 mmol) in THF (2 ml) and diisopropylethylamine (155 μl, 0.89 mmol). The mixture was stirred for 2 h and evaporated in vacuo. The residue was purified by flash column chromatography on silica (eluant EtOAc:pet. ether 80:20 to EtOAc 100%) to give a white solid; yield 268 mg, 57%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08063038B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-9d4f0adc2d9c4e179ec65e9e6d1e3b4e |
| Source note | uspto-grants-2011_11 |