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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253695Generated: October 31, 2026

Sodium hydride → Methyl-6-chloro-3-(4-ethylphenylamino)benzo[d]isoxazole-7-carboxylate

https://huagongshe.com/reaction/253695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantHCID 178436606HCID 178436606—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductMethyl-6-chloro-3-(4-ethylphenylamino)benzo[d]isoxazole-7-carboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872128B2
Source datasetuspto-grants-2011_01
ORD IDord-d91eb9f687cc4fed95ebfddffc6575bc
Source noteuspto-grants-2011_01