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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 22319565 | HCID 22319565 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(6-(3,5-dichlorophenyl)-1H-indazol-3-yl)butyramide | HCID 22319691 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06949579B2 |
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| Source dataset | uspto-grants-2005_09 |
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| ORD ID | ord-9fdf3097c5e74ccca04d34f4aede8a58 |
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| Source note | uspto-grants-2005_09 |
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