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HRID 542638作成日:2026年10月27日

Cyclopropylamine → 9-Carbamoyl-9-(3-cyclopropylaminopropyl)fluorene

https://huagongshe.com/reaction/542638

反応式

関与物質

役割名称HCID仕込み量
反応物CyclopropylamineHCID 69828—
反応物Maleic AcidHCID 444266—
反応物9-(2-Cyanoethyl)-9H-fluorene-9-carboxamideHCID 3018819—
反応物9-Carbamoyl-9-(3-cyclopropylaminopropyl)fluorene maleateHCID 70442802—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
溶媒Ethyl AcetateHCID 8857—
生成物9-Carbamoyl-9-(3-cyclopropylaminopropyl)fluoreneHCID 13853491—

反応条件

温度25 °C

反応手順

A solution of 4.6 g. of 9-carbamoyl-9-(2-cyanoethyl)fluorene in 200 ml. of ethanol containing 2.3 g. of 5% palladium on carbon and 10.0 g. of cyclopropylamine was stirred under hydrogen at 60 psi at 90° C. for sixteen hours. The reaction mixture was cooled to 25° C., filtered and concentrated to a volume of 20 ml. The oil was dissolved in 200 ml. of 50% ethyl acetate-diethyl ether and the solution was extracted with 6N hydrochloric acid. The acid layer was cooled and made alkaline by addition of 10% aqueous sodium hydroxide. The alkaline solution was extracted several times with fresh diethyl ether-ethyl acetate. The organic extracts were combined, washed with water, dried and the solvent was removed by evaporation to give 3.7 g. of the title comound as an oil. The oil was diluted by addition of 1.4 g. of maleic acid and the mixture was further diluted by addition of 50 ml. of ethyl acetate. The precipitated crystals were collected by filtration and dried to afford 1.5 g. of 9-carbamoyl-9-(3-cyclopropylaminopropyl)fluorene maleate. m.p. 163°-165° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04658061
出典データセットuspto-grants-1987_04
ORD IDord-ec8246ab8aa8491694a98456405c4a39
出典メモuspto-grants-1987_04