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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 542638생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/542638

반응식

참여 물질

역할이름HCID투입량
반응물CyclopropylamineHCID 69828—
반응물Maleic AcidHCID 444266—
반응물9-(2-Cyanoethyl)-9H-fluorene-9-carboxamideHCID 3018819—
반응물9-Carbamoyl-9-(3-cyclopropylaminopropyl)fluorene maleateHCID 70442802—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
용매Ethyl AcetateHCID 8857—
생성물9-Carbamoyl-9-(3-cyclopropylaminopropyl)fluoreneHCID 13853491—

반응 조건

온도25 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04658061
출처 데이터셋uspto-grants-1987_04
ORD IDord-ec8246ab8aa8491694a98456405c4a39
출처 메모uspto-grants-1987_04