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HRID 1702102作成日:2026年10月26日

Hydrochloric Acid → 1-(2-Formamidophenyl)-1'-methylspiro[indoline-3,4'-piperidine] hydrochloride

https://huagongshe.com/reaction/1702102

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Sodium MethoxideHCID 10942334—
反応物1-(2-Aminophenyl)-1'-methylspiro[indoline-3,4'-piperidine]dihydrochlorideHCID 12801598—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
生成物1-(2-Formamidophenyl)-1'-methylspiro[indoline-3,4'-piperidine] hydrochlorideHCID 12801604—

反応条件

温度90 °C

反応手順

To a mixture of 15.0 g of 1-(2-aminophenyl)-1'-methylspiro-[indoline-3,4'-piperidine] dihydrochloride, Example 16, in 75 ml of dimethylformamide at 90° C. under nitrogen is added 8.6 g of sodium methoxide. Following this addition the reaction temperature is increased to 110°-115° C. and maintained at this temperature for 40 minutes. The resulting dark brown mixture is permitted to cool to 90° C. and then poured onto 800 ml of ice-water. The mixture is filtered and the filter cake is washed with water and then dissolved in chloroform. The chloroform solution is successively washed with brine, dried and concentrated leaving a red colored glass. The glass is dissolved in ether, where it is converted to its hydrochloric acid salt which is collected by filtration and then washed with ether and finally dried. The salt is recrystallized from a methyl alcohol-ether mixture to provide the product, mp 287.5° C., dec of 1-(2-formamidophenyl)-1'-methylspiro[indoline-3,4'-piperidine] hydrochloride.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04379933
出典データセットuspto-grants-1983_04
ORD IDord-3b0f39c53da247baadc6220375b8124a
出典メモuspto-grants-1983_04