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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793654Generated: October 26, 2026

Ammonia → Zonisamide

https://huagongshe.com/reaction/1793654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant1,2-Benzisoxazole-3-methanesulfonate sodiumHCID 23674934—
Solvent1,2-DichloroethaneHCID 11—
SolventTriethylamineHCID 8471—
ProductZonisamideHCID 5734—

Reaction Steps

Water is removed by distillation from the above mixture of 1,2-benzisoxazole-3-acetic acid and 1,2-dichloroethane, and thereto is added dropwise chlorosulfonic acid (15.5 g) while the internal temperature is kept at 63° C.–79° C. After the addition, the mixture is stirred for 90 minutes while the reaction temperature is kept at 63° C.–79° C. After cooling, a 25% aqueous sodium hydroxide solution is added to the reaction mixture so as to adjust the pH value thereof to pH 11 or above. Water is removed by distillation from the reaction mixture to give a mixture of sodium 1,2-benzisoxazole-3-methanesulfonate and 1,2-dichloroethane. Triethylamine (2.4 g) and phosphoryl chloride (17.5 g) are added to this mixture, and the mixture is stirred at a temperature of 77° C.–83° C. for 6 hours. After cooling, to the reaction mixture is added 1,2-dichloroethane (80 ml), and ammonia gas is blown into the mixture until saturated while the reaction temperature is kept at 30° C.–60° C. The reaction mixture is concentrated, and water is added thereto. The mixture is stirred, and the precipitated crystals are collected by filtration, and washed with water to give crude crystals of 1,2-benzisoxazole-3-methanesulfonamide. The purity of the crude crystals is 96%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07081539B2
Source datasetuspto-grants-2006_07
ORD IDord-0350bb6b14d0439995b609b641c91c4c
Source noteuspto-grants-2006_07