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HRID 2305772作成日:2026年10月25日

Acetic Anhydride → 5-Amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(2,5-dimethylbenzoyl)-3-ethoxypyrazole

https://huagongshe.com/reaction/2305772

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AnhydrideHCID 7918—
反応物TriethylamineHCID 8471—
反応物Tetraethyl orthocarbonateHCID 66213—
反応物[2,6-Dichloro-4-(trifluoromethyl)phenyl]hydrazineHCID 688223—
反応物2,5-DimethylbenzoylacetonitrileHCID 15895264—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物5-Amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(2,5-dimethylbenzoyl)-3-ethoxypyrazoleHCID 12972143—

反応手順

A solution of 0.26 g (1.5 mmol) of 2,5-dimethylbenzoylacetonitrile, 0.34 mL (0.31 g, 1.60 mmol) of tetraethylorthocarbonate and 0.30 mL (0.33 g, 3.20 mmol) of acetic anhydride in 10 mL of EtOAc was refluxed overnight. The solvent was evaporated and 10 mL of absolute ethanol was added and then stripped. The residues were dissolved in 10 mL of ethanol, 368 mg (1.5 mmol) of 2,6-dichloro-4-trifluoromethylphenyl-hydrazine and 0.7 mL (0.51 g, 5.0 mmol) of triethylamine were added, and the mixture was refluxed for 90 minutes. The mixture was poured into water, extracted with EtOAc and the organic extracts were washed with dilute HCl and brine, and dried over MgSO4. Evaporation gave a gum which was chromatographed on silica gel with 4:1 hexane/EtOAc to give the title product which crystallized from pentane, 15 mg (2%), m.p. 99-101° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06441018B2
出典データセットuspto-grants-2002_08
ORD IDord-565015cbebf34cddae89b639ede9bccf
出典メモuspto-grants-2002_08