HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butylamine → N-tert-butyl-2-(1H-indazol-5-yl)-3-[methyl(propan-2-yl)amino]quinoxaline-6-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Propylphosphonic anhydride | HCID 111923 | — |
| Reactant | 2-(1H-indazol-5-yl)-3-(isopropyl(methyl)amino)quinoxaline-6-carboxylic acid | HCID 50991659 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-tert-butyl-2-(1H-indazol-5-yl)-3-[methyl(propan-2-yl)amino]quinoxaline-6-carboxamide | HCID 70654225 | — |
Reaction Steps
To a solution of 2-(1H-indazol-5-yl)-3-[methyl(propan-2-yl)amino]quinoxaline-6-carboxylic acid (200 mg, 0.55 mmol) in dichloromethane (30 ml) was added triethylamine (210 mg, 2.08 mmol), 2-methylpropan-2-amine (121 mg, 1.65 mmol), and T3P (396 mg, 1.25 mmol), and the resulting mixture was stirred for 1 h at room temperature. The solution was diluted with water (150 ml), extracted with dichloromethane (3×50 ml), dried over anhydrous magnesium, and concentrated in vacuo to get N-tert-butyl-2-(1H-indazol-5-yl)-3-[methyl(propan-2-yl)amino]quinoxaline-6-carboxamide as a yellow solid (311 mg, crude).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08916561B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-f55e8946de4440fa9cd57b867f101943 |
| Source note | uspto-grants-2014_12 |