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HRID 2198487作成日:2026年10月26日

Dimethylformamide → N-(1-Ethyl-3-piperidyl)-4-(8-trifluoromethyl-4-quinolylamino)benzamide

https://huagongshe.com/reaction/2198487

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Sodium CarbonateHCID 10340—
反応物3-amino-N-ethylpiperidineHCID 98094—
反応物4-(8-Trifluoromethyl-4-quinolylamino)benzoic acid hydrochloride monohydrateHCID 70545502—
触媒Thionyl ChlorideHCID 24386—
溶媒WaterHCID 962—
溶媒ChloroformHCID 6212—
生成物N-(1-Ethyl-3-piperidyl)-4-(8-trifluoromethyl-4-quinolylamino)benzamideHCID 2052013937%

反応手順

11.6 Grams (0.03 mole) of 4-(8-trifluoromethyl-4-quinolylamino)benzoic acid hydrochloride monohydrate were refluxed in thionyl chloride containing a few drops of dimethyl formamide for one hour. The thionyl chloride was evaporated and 50 milliliters of benzene were added and evaporated. The resulting acid chloride hydrochloride was added in portions with stirring to a cooled mixture of 3.84 grams (0.03 mole) of 3-amino-1-ethylpiperidine in 80 milliliters of chloroform and 31.8 grams (0.3 mole) of sodium carbonate in 100 milliliters of water. The product began to precipitate almost at once, and the mixture was stirred vigorously for two hours, and allowed to stand overnight. Filtration gave a solid which was stirred in water, collected and dried. The resulting solid was dissolved in an ethanol:chloroform mixture and chromatographed on an alumine column made up in chloroform. Elution with chloroform gave 4.9 grams (37%) of title compound as a pale yellow solid, melting point 177°-178° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04357333
出典データセットuspto-grants-1982_11
ORD IDord-3328dc48c13a419da6dfce9ddbcfcab7
出典メモuspto-grants-1982_11