Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 66617677 | HCID 66617677 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | HCID 66617763 | HCID 66617763 | — |
Reaction Steps
To a solution of 200 mg of 2-(2-cyclopropyl)-6-nitro-3-oxo-4H-benz[1,4]oxazine (1 g) in EtOH/water (20 mL; 2:1 v/v) was added 5 eq of iron and 5 eq of ammonium chloride and the reaction was heated at 90° C. for 4 h. The reaction mixture was cooled to room temperature, diluted with dichloromethane and filtered. The layers were separated, the aqueous was extracted once with dichloromethane, the combined organics layers were dried over magnesium sulfate, the solution filtered and the filtrate evaporated in vacuo to give the desired product 6-amino-2-(2-cyclopropyl)-3-oxo-4H-benz[1,4]. MS (m/e): 191 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07851480B2 |
|---|
| Source dataset | uspto-grants-2010_12 |
|---|
| ORD ID | ord-4b1eee1b1c0d4d96848efddd60e72303 |
|---|
| Source note | uspto-grants-2010_12 |
|---|