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HRID 1660367作成日:2026年10月26日

Triethanolamine → 1-[2-(Ethoxycarbonyl)aminophenyl]-1'-methylspiro[indoline-3,4'-piperidine]

https://huagongshe.com/reaction/1660367

反応式

関与物質

役割名称HCID仕込み量
反応物TriethanolamineHCID 7618—
反応物Ethyl chloroformateHCID 10928—
反応物1-(2-Aminophenyl)-1'-methylspiro[indoline-3,4'-piperidine]dihydrochlorideHCID 12801598—
溶媒ChloroformHCID 6212—
生成物1-[2-(Ethoxycarbonyl)aminophenyl]-1'-methylspiro[indoline-3,4'-piperidine]HCID 12801608—

反応手順

A slurry of 10.36 g of 1-(2-aminophenyl)-1'-methylspiro[indoline-3,4'-piperidine]dihydrochloride of Example 1b in 60 ml of chloroform is treated portionwise with 12.3 ml of triethanolamine. The resulting mixture is cooled in an ice bath and treated dropwise over 40 minutes with a solution of 2.7 ml of ethyl chloroformate in 20 ml of chloroform. After stirring at room temperature for 1 hour, an additional 3.0 ml of ethyl chloroformate is added and the mixture is permitted to stand 16 hours. The product is washed thrice with water, brine, dried over anhydrous sodium sulfate, concentrated and pumped on under high vacuum to give a crude carbamate. Chromatography on silica gel (100 g) using ether-methylene chloride affords an oil. The material crystallizes on prolonged standing to yield 1-[2-(ethoxycarbonyl)aminophenyl]-1'-methylspiro[indoline-3,4'-piperidine], mp 99.5°-101.0° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04307235
出典データセットuspto-grants-1981_12
ORD IDord-32ed2725ab6a472288674baea068fbd2
出典メモuspto-grants-1981_12