HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → Methyl-6-chloro-3-(4-ethylphenylamino)benzo[d]isoxazole-7-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178436606 | HCID 178436606 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl-6-chloro-3-(4-ethylphenylamino)benzo[d]isoxazole-7-carboxylate | HCID 59805810 | — |
Reaction Steps
To a solution of methyl-6-chloro-3-(N-(4-ethylphenyl)-N′-hydroxycarbamimidoyl)-2-fluorobenzoate (225 mg, 641 μmol) in DMF (6.4 ml) chilled to 0° C. was added NaH (17 mg, 706 μmol) in one portion. The yellow solution evolved gas and immediately turned a dark orange color. After 20 min, the mixture was diluted with H2O and DCM, the layers were separated and the aqueous layer was extracted with DCM (2×). The organic layers were combined and washed with brine, dried over MgSO4, filtered and concentrated to provide the title compound as a light brown solid, which was used for the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07872128B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-d91eb9f687cc4fed95ebfddffc6575bc |
| Source note | uspto-grants-2011_01 |