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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 512569Generated: November 1, 2026

Riluzole → N1-[6-(trifluoromethoxy)-1,3-benzothiazol-2-yl]-2-2-methoxy-5-[(E)-3-oxo-3-(3,4,5-trimethoxyphenyl)-1-propenyl]phenoxyacetamide

https://huagongshe.com/reaction/512569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantRiluzoleHCID 5070—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant2-{2-methoxy-5-[(E)-3-oxo-3-(3,4,5-trimethoxy phenyl)-1-propenyl]phenoxy}acetic acidHCID 56968190—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN1-[6-(trifluoromethoxy)-1,3-benzothiazol-2-yl]-2-2-methoxy-5-[(E)-3-oxo-3-(3,4,5-trimethoxyphenyl)-1-propenyl]phenoxyacetamideHCID 60148075805.1%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 6-(trifluoromethoxy)-2-aminobenzothiazole (234 mg, 1.0 mmol) in dichloromethane (20 mL) was added 1-Ethyl-3-(3-Dimethylaminopropyl)carbodiimide (EDC) (191 mg, 1.0 mmol) and 1-hydroxy-1,2,3-benzotriazole (HOBt) (13.5 mg, 0.1 mmol). Then added 2-{2-methoxy-5-[(E)-3-oxo-3-(3-(3,4,5-trimethoxy phenyl)-1-propenyl]phenoxy}acetic acid (2) (402 mg, 0.1 mmol) and the reaction mixture was stirred at a temperature of 25° C. for 24 h and the reaction was monitored by TLC. Then to this water is added and extracted with dichloromethane. The solvent was evaporated under vacuum to afford the crude product. This was further purified by column chromatography using ethyl acetate and hexane as solvent system to obtain the pure product (9j) (498 mg, 80% yield)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102638B2
Source datasetuspto-grants-2015_08
ORD IDord-4d1fa148c6224528bfa6dd059f96ac31
Source noteuspto-grants-2015_08