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HRID 329022作成日:2026年10月25日

Potassium Iodide → (+/-)-5-(trans-1,2,3,4,4a,8,9,14a-Octahydropyrido[4',3':2,3]indolo[1,7-ab][1]benzazepin-3-yl)-2-pentanone

https://huagongshe.com/reaction/329022

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物TriethylamineHCID 8471—
反応物2-(3-Chloropropyl)-2-methyl-1,3-dioxolaneHCID 80079—
反応物HCID 12752824HCID 12752824—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物(+/-)-5-(trans-1,2,3,4,4a,8,9,14a-Octahydropyrido[4',3':2,3]indolo[1,7-ab][1]benzazepin-3-yl)-2-pentanoneHCID 86734690—

反応条件

温度62 °C

反応手順

3.6 grams of potassium iodide and 12 ml. of triethylamine were added to a solution of 5.5 grams of (±)-trans-1,2,3,4,4a,8,9,14a-octahydropyrido[4',3':2,3]=indolo[1,7-ab][1]benzazepine in 50 ml. DMF, followed by addition of 3.7 grams of 5-chloro-2-pentanone ethylene ketal. The mixture was heated at approximately 62° C for 20 hours. The mixture was then poured into water, extracted with benzene, and chromatographed through basic alumina to eliminate remaining benzazepine starting material. The resulting ketal was dissolved in ether. HCl gas was bubbled through this solution to precipitate the hydrochloride salt of the title compound. Recrystallization from ethanol yielded 350 mg. of the title compound, hydrochloride salt, m.p. 258°-259° C(dec).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04018930
出典データセットuspto-grants-1977_04
ORD IDord-eefc34aa945b440da2ec42f1a254114a
出典メモuspto-grants-1977_04