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HRID 1607003作成日:2026年10月27日

Propargyl ether → 8-fluoro-4,5-dihydro-3-(3-methoxy-1-propynyl)-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one

https://huagongshe.com/reaction/1607003

反応式

関与物質

役割名称HCID仕込み量
反応物Propargyl etherHCID 23349—
反応物8-fluoro-4,5-dihydro-3-iodo-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-oneHCID 19830685—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒HCID 178418476HCID 178418476—
溶媒DiethylamineHCID 8021—
生成物8-fluoro-4,5-dihydro-3-(3-methoxy-1-propynyl)-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-oneHCID 19851532—

反応手順

7 g (19.9 mmol) of 8-fluoro-4,5-dihydro-3-iodo-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one was heated to boiling under reflux for 3 hours with 2.5 ml (29 mmol) of propargyl ether, 100 mg of bis-(triphenylphosphine)-palladium(II) dichloride and 30 mg of copper(I) iodide in 70 ml of diethylamine. The reaction mixture was evaporated and the residue was chromatographed on silica gel while eluting with ethyl acetate. After recrystallization from ethyl acetate there was obtained 8-fluoro-4,5-dihydro-3-(3-methoxy-1-propynyl)-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one of melting point 146°-147°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04863920
出典データセットuspto-grants-1989_09
ORD IDord-b95a591d0ef241dc8451003988a85546
出典メモuspto-grants-1989_09