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HRID 2198488作成日:2026年10月25日

Dimethylformamide → N-(2-diethylaminoethyl)-N-ethyl-4-(8-trifluoromethyl-4-quinolylamino)benzamide

https://huagongshe.com/reaction/2198488

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TriethylethylenediamineHCID 66040—
反応物4-(8-Trifluoromethyl-4-quinolylamino)benzoic acid hydrochloride monohydrateHCID 70545502—
触媒Thionyl ChlorideHCID 24386—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒ChloroformHCID 6212—
生成物N-(2-diethylaminoethyl)-N-ethyl-4-(8-trifluoromethyl-4-quinolylamino)benzamideHCID 2052014964%

反応手順

11.6 Grams (0.03 mole) of 4-(8-trifluoromethyl-4-quinolylamino)benzoic acid hydrochloride monohydrate were refluxed in 80 milliliters of thionyl chloride containing two drops of dimethyl formamide for 11/2 hours. The thionyl chloride was evaporated off 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 4.32 grams (0.03 mole) of N,N,N'-triethyl ethylenediamine in 80 milliliters of chloroform and 31.8 grams (0.3 mole) of sodium carbonate in 100 milliliters of water. The mixture was stirred for one hour, and allowed to stand overnight. The chloroform layer was separated and dried and the chloroform evaporated to give a gummy solid, which was largely taken up in ether. On concentration of this solution a colourless solid crystallised out, which was collected to give 8.8 grams (63% yield) of N-(2-diethylaminoethyl)-N-ethyl-4-(8-trifluoromethyl-4-quinolylamino)benzamide quarter hydrate, m.p. 151°-152° 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-040fa951ae274dd09b72d85c9cc46476
出典メモuspto-grants-1982_11