HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2,2-difluoro-4-methyl-7-nitro-4H-1,4-benzoxazin-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,2-difluoro-7-nitro-4H-1,4-benzoxazin-3-one | HCID 21878155 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2,2-difluoro-4-methyl-7-nitro-4H-1,4-benzoxazin-3-one | HCID 21878106 | — |
Reaction Steps
To a stirred suspension of 2,2-difluoro-7-nitro-4H-1,4-benzoxazin-3-one (WO 99/40094, 2.16 g, 9.38 mmol) in DMF (10 mL) is added K2CO3 (1.94 g, 14.07 mmol) followed by addition of MeI (0.87 mL, 14.07 mmol). The resulting solution is stirred over night at room temperature. To this reaction mixture is added water (50 mL), and the resulting solution is extracted with EtOAc (50 mL×3). The combined organic phases are washed with water (50 mL) and saline (50 mL), dried over Na2SO4 and concentrated under reduced pressure to give the title compound that is purified by passing through a short silica gel column with EtOAc (1.3 g, 57%), 1H NMR (300 MHz, DMSO) δ 8.25–8.17 (m, 2H), 7.62 (d, 1H), 3.47 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07141588B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-6fd2f78d11e24e498e7a6a118a5640e8 |
| Source note | uspto-grants-2006_11 |