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HRID 247249作成日:2026年10月24日

Salicylamide → 5-Chloro-2-[(1-methyl-3-pyrrolidinyl)oxy]benzamide hemihydrate

https://huagongshe.com/ja/reaction/247249

反応式

関与物質

役割名称HCID仕込み量
反応物SalicylamideHCID 5147—
反応物Sodium hydrideHCID 24758—
反応物5-Chloro-2-hydroxybenzamideHCID 348094—
反応物3-Bromo-1-methylpyrrolidineHCID 13726279—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物5-Chloro-2-[(1-methyl-3-pyrrolidinyl)oxy]benzamide hemihydrateHCID 7039369834.1%

反応手順

To a cooled suspension of 2.4 g (0.41 mole) sodium hydride in 50 ml of dimethylformamide was added dropwise 17 g (0.1 mole) of 5-chlorosalicylamide dissolved in 50 ml of dimethylformamide at a rate such that the temperature did not exceed 20° C. After addition of the salicylamide was complete, 16.7 g (0.1 mole) of 3-bromo-1-methylpyrrolidine dissolved in 50 ml of dimethylformamide was added dropwise. The reaction mixture was stirred and heated at reflux for 19 hr. The cooled solution was diluted with 250 ml of water and extracted twice with 250 ml portions of chloroform. The chloroform was extracted thrice with 500 ml portions of 3N hydrochloric acid. The aqueous extracts were made alkaline with 50% sodium hydroxide and extracted with ethyl acetate. Drying over magnesium sulfate and evaporation of the ethyl acetate under reduced pressure gave 6 g (23%) of product as a beige solid. The solid was recrystallized from ethyl acetate, m.p. 126°-128° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04705853
出典データセットuspto-grants-1987_11
ORD IDord-c1213d82102941b990e8fde8dc761705
出典メモuspto-grants-1987_11