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HRID 1586202作成日:2026年10月26日

Hydrochloric Acid → N-[2-methyl-3-(2-phthalimidylethyl)-1H-indol-5-yl]-4-fluoro-benzamide

https://huagongshe.com/reaction/1586202

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HexaneHCID 8058—
反応物2-(4-Oxopentyl)-1H-isoindole-1,3(2H)-dioneHCID 236270—
反応物4-(4-Fluorobenzoyl)aminophenylhydrazineHCID 11831684—
溶媒EthanolHCID 702—
生成物N-[2-methyl-3-(2-phthalimidylethyl)-1H-indol-5-yl]-4-fluoro-benzamideHCID 232904766.6%

反応条件

温度80 °C

反応手順

To a solution of 5.33 gm (21.7 mMol) 4-(4-fluorobenzoyl)aminophenylhydrazine and 5.03 gm (21.8 mMol) 5-phthalimidyl-2-pentanone in 100 mL ethanol were added 2 mL concentrated hydrochloric acid and the reaction mixture was heated at 80° C. for 14 hours. To the reaction mixture were then added an additional 3 mL concentrated hydrochloric acid and heating continued for an additional 6 hours. The reaction mixture was then cooled to 0° C. and 100 mL hexane were slowly added. The solid which formed was filtered and washed with hexane and provided, after drying, 6.67 gm of the desired compound. The mother liquor was concentrated under reduced pressure and then subjected to silica gel chromatography, eluting with 1:1 hexane:ethyl acetate. Fractions containing product were combined and concentrated under reduced pressure to provide an additional 0.63 gm of product. Overall yield was 7.3 gm (76%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05942536
出典データセットuspto-grants-1999_08
ORD IDord-819c94266a2841929f7934dcc8ce59c6
出典メモuspto-grants-1999_08