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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 850921생성일: 2026년 10월 25일

Isopropylamine → Indecainide

https://huagongshe.com/reaction/850921

반응식

참여 물질

역할이름HCID투입량
반응물IsopropylamineHCID 6363—
반응물9-(2-Cyanoethyl)-9H-fluorene-9-carboxamideHCID 3018819—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
생성물IndecainideHCID 5219560%

반응 조건

온도100 °C

반응 단계

A mixture of 500 g. of 9-aminocarbonyl-9-(2-cyanoethyl)fluorene, 1500 ml. of isopropylamine and 100 g. of 5% palladium on carbon was placed in a one gallon high pressure hydrogenation bomb. The bomb was pressurized with hydrogen to a pressure of 1500 psi, and the reaction mixture was then stirred at 100° C. for ten hours, and for an additional eight hours at room temperature. The reaction mixture was filtered to remove the hydrogenation catalyst, and the solvent was removed from the filtrate by evaporation under reduced pressure. The residue was dissolved in ethyl acetate, and the solution was extracted several times with 1 N hydrochloric acid. The acidic extracts were combined, made alkaline by the addition of sodium hydroxide, and the alkaline mixture was extracted with fresh ethyl acetate. The organic layer was separated, washed with water and dried. Removal of the solvent by evaporation under reduced pressure provided 9-(3-isopropylaminopropyl)-9-aminocarbonylfluorene as a solid residue. The solid was dissolved in methanol and treated with anhydrous hydrogen chloride. The crystalline product which formed was recrystallized from chloroform to afford 391 g. of 9-(3-isopropylaminopropyl)-9-aminocarbonylfluorene hydrochloride. Yield 60%. m.p. 216.5°-217° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04382093
출처 데이터셋uspto-grants-1983_05
ORD IDord-d0b858b19265490f8cc2a03d9c9b9882
출처 메모uspto-grants-1983_05