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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519405Generated: October 27, 2026

Ethyl Acetate → N-[4-(Aminosulfonyl)-2-methylphenyl]-7-methoxy-2-oxo-8-propyl-2H-chromene-3-carboxamide

https://huagongshe.com/reaction/1519405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Amino-3-methylbenzene-1-sulfonamideHCID 143037—
ReactantPropylphosphoric anhydrideHCID 16167369—
Reactant7-methoxy-2-oxo-8-propyl-2H-chromene-3-carboxylic acidHCID 59362330—
SolventDichloromethaneHCID 6344—
ProductN-[4-(Aminosulfonyl)-2-methylphenyl]-7-methoxy-2-oxo-8-propyl-2H-chromene-3-carboxamideHCID 52932182—

Reaction Steps

To a solution of Intermediate 1 (0.10 g, 0.381 mmol) in CH2Cl2 (5.0 mL) was added diisopropyl ethyl amine (0.1 mL, 0.572 mmol) and a 50% solution of propylphosphonic anhydride in ethyl acetate (0.340 mL, 0.572 mmol). The mixture was stirred for 30 minutes at room temperature. 4-Amino-3-methylbenzenesulfonamide [CAS # 53297-70-4] (0.071 g, 0.381 mmol) was added to the reaction mixture at room temperature and stirred overnight. The reaction mixture was then poured onto ice water (25 mL) and CH2Cl2 (25 mL) added. The organic layer was separated and washed with brine (25 mL), dried with Na2SO4, filtered and concentrated to dryness. The residue was triturated with CH2Cl2/Hexanes and then the solid was purified with a MPLC to give the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073888B2
Source datasetuspto-grants-2015_07
ORD IDord-946c9e10ea954933a1f2af04e922051f
Source noteuspto-grants-2015_07