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HRID 132511作成日:2026年10月25日

Hydrochloric Acid → 5-{3-[1-(2-Fluoro-5-trifluoromethylphenyl)-cyclopropyl]-2-oxo-propionylamino}-phthalide

https://huagongshe.com/reaction/132511

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Thionyl ChlorideHCID 24386—
反応物5-AminophthalideHCID 720669—
反応物3-[1-(2-Fluoro-5-trifluoromethylphenyl)-cyclopropyl]-2-oxo-propionic acidHCID 68841516—
溶媒Ethyl AcetateHCID 8857—
溶媒DimethylacetamideHCID 31374—
生成物5-{3-[1-(2-Fluoro-5-trifluoromethylphenyl)-cyclopropyl]-2-oxo-propionylamino}-phthalideHCID 68871207—

反応条件

温度0 °C

反応手順

At −10° C., 0.84 ml of thionyl chloride are added to 2.9 g of 3-[1-(2-fluoro-5-trifluoromethylphenyl)-cyclopropyl]-2-oxo-propionic acid in 15 ml dimethylacetamide. The mixture is stirred for 30 min. at −10° C. and for 1 hour at 0° C. and then added to 1.95 g of 5-aminophthalide (or, vice versa, 5-aminophthalide may be added to the mixture). After 16 hours at ambient temperature, 2 M hydrochloric acid and ethyl acetate are added, the organic phase is washed to neutral with water, dried over sodium sulfate and concentrated. After chromatography on silica gel (hexane/ethyl acetate: 1+1) and recrystallization from diisopropyl ether, 2.4 g of 5-{3-[1-(2-fluoro-5-trifluoromethylphenyl)-cyclopropyl]-2-oxo-propionylamino}-phthalide (m.p. 168° C.) are obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07388006B2
出典データセットuspto-grants-2008_06
ORD IDord-0d1bfca890c446e988feafadab5cd626
出典メモuspto-grants-2008_06