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HRID 2198485作成日:2026年10月27日

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

https://huagongshe.com/reaction/2198485

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物TriethylethylenediamineHCID 66040—
反応物2-(8-Trifluoromethyl-4-quinolylamino)benzoic acid hydrochloride dihydrateHCID 70546379—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒ChloroformHCID 6212—
溶媒Thionyl ChlorideHCID 24386—
生成物N-(2-diethylaminoethyl)-N-ethyl-2-(8-trifluoromethyl-4-quinolylamino)benzamideHCID 2052014046.2%

反応手順

12.1 Grams (0.03 mole) of 2-(8-trifluoromethyl-4-quinolylamino)benzoic acid hydrochloride dihydrate were refluxed in 80 milliliters of thionyl chloride for half an hour. A yellow solid precipitated. 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'-triethylethylenediamine 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 an oil, which could not be solidified. The oil was dissolved in ether and purified by chromatography on an alumina (type H) column. Elution with ether/chloroform (50:50) gave a pale yellow oil which was kept under vacuum for four days when it gradually solidified to give 6.35 grams (46% yield) of title compound of melting point 112°-113° 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-dd65826eaac2415690c96a7254070999
出典メモuspto-grants-1982_11