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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497635Generated: October 28, 2026

Ethyl Acetate → N-(6-(3,5-dichlorophenyl)-1H-indazol-3-yl)butyramide

https://huagongshe.com/reaction/497635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 22319565HCID 22319565—
SolventTetrahydrofuranHCID 8028—
ProductN-(6-(3,5-dichlorophenyl)-1H-indazol-3-yl)butyramideHCID 22319691—

Reaction Conditions

Temperature65 °C

Reaction Steps

11.2 cm3 of tetrabutylammonium fluoride as a 1M solution in tetrahydrofuran are added to 1 g of N-[6-(3,5-dichlorophenyl)-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-indazol-3-yl]butanamide, described previously, in 20 cm3 of tetrahydrofuran, the reaction medium is then heated at about 65° C. for 18 hours and the heating is stopped to add 75 cm3 of ethyl acetate. The organic phase is washed with 2×50 cm3 of saturated aqueous sodium hydrogen carbonate solution and then with 50 cm3 of saturated aqueous sodium chloride solution. The organic phase is dried over magnesium sulphate, filtered and evaporated under reduced pressure (2 kPa; 50° C.). After drying (90 Pa; 50° C.), 290 mg of N-[6-(3,5-dichlorophenyl)-1H-indazol-3-yl]butanamide are obtained in the form of a white product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06949579B2
Source datasetuspto-grants-2005_09
ORD IDord-9fdf3097c5e74ccca04d34f4aede8a58
Source noteuspto-grants-2005_09