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HRID 523280作成日:2026年10月26日

1,3-Diethyl 2-(3-oxocyclohexyl)propanedioate → 5-bromo-2-(1,3-diethoxy-1,3-dioxopropan-2-yl)-6-fluoro-2,3,4,9-tetrahydro-1H-carbazole-8-carboxylic acid

https://huagongshe.com/reaction/523280

反応式

関与物質

役割名称HCID仕込み量
反応物1,3-Diethyl 2-(3-oxocyclohexyl)propanedioateHCID 317049—
反応物4-Bromo-5-fluoro-2-hydrazinylbenzoic acid hydrochlorideHCID 76848196—
溶媒Acetic AcidHCID 176—
生成物5-bromo-2-(1,3-diethoxy-1,3-dioxopropan-2-yl)-6-fluoro-2,3,4,9-tetrahydro-1H-carbazole-8-carboxylic acidHCID 11776109049%

反応手順

A solution of diethyl 2-(3-oxocyclohexyl)malonate (15.26 g, 59.5 mmol) and 4-bromo-5-fluoro-2-hydrazinylbenzoic acid hydrochloride [Intermediate 24B] (17.0 g, 59.5 mmol) in acetic acid (120 mL) was heated at reflux for 2 h, then was stirred overnight at room temperature. The precipitate which formed was collected by filtration to provide a white solid. The filtrate was concentrated and purified by column chromatography on silica gel (80 g), eluting with EtOAc-hexanes (gradient from 0-100%). The resulting oily product was crystallized from a mixture of EtOAc, ether and hexanes to provide additional solid, which was combined with the first solid to provide 5-bromo-2-(1,3-diethoxy-1,3-dioxopropan-2-yl)-6-fluoro-2,3,4,9-tetrahydro-1H-carbazole-8-carboxylic acid as a white solid (10.5 g, 49% yield). Mass spectrum m/z 470, 472 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09334290B2
出典データセットuspto-grants-2016_05
ORD IDord-9d6c9d1b33d246e588d4c05344625996
出典メモuspto-grants-2016_05