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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643985Generated: October 27, 2026

6-Methylanthranilic acid → 2-Methyl-6-[4-(5-methyl-2-phenyl-oxazol-4-ylmethoxy)-benzenesulfonylamino]-benzoic acid

https://huagongshe.com/reaction/643985

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Methylanthranilic acidHCID 151210—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(5-Methyl-2-phenyl-oxazol-4-ylmethoxy)-benzenesulfonyl chlorideHCID 21090679—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-Methyl-6-[4-(5-methyl-2-phenyl-oxazol-4-ylmethoxy)-benzenesulfonylamino]-benzoic acidHCID 11352042—

Reaction Conditions

Temperature60 °C

Reaction Steps

Sodium bicarbonate (159 mg, 1.89 mmol) and 2-amino-6-methylbenzoic acid (95.5 mg, 0.63 mmol) are dissolved in a mixture of 1 mL of THF and 1.5 mL of water and heated to 60° C. A solution of the title C compound, 4-(5-methyl-2-phenyl-oxazol-4-ylmethoxy)-benzenesulfonyl chloride (200 mg, 0.55 mmol) in 1 mL of THF is then added dropwise. The mixture is heated for an additional 2 h at 60° C., after which most of the THF is removed by passing a stream of nitrogen gas over the solution. The residue is partitioned between EtOAc and 1 N aqueous HCl. The organic phase is dried over anhydrous magnesium sulfate, filtered, and concentrated under vacuum to give crude product which is purified by chromatography on silica gel with an EtOAc (15%)-hexane (85%) mixture (containing 0.5% formic acid) as the eluent to give 2-methyl-6-[4-(5-methyl-2-phenyl-oxazol-4-ylmethoxy)-benzenesulfonylamino]-benzoic acid as a white solid: m.p. 167-170° C.; ESI-MS 479 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700637B2
Source datasetuspto-grants-2010_04
ORD IDord-fc4aae9e22b44da7b613dad9a540cc94
Source noteuspto-grants-2010_04