돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 523280생성일: 2026년 10월 24일

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/ko/reaction/523280

반응식

참여 물질

역할이름HCID투입량
반응물1,3-Diethyl 2-(3-oxocyclohexyl)propanedioateHCID 317049—
반응물4-Bromo-5-fluoro-2-hydrazinylbenzoic acid hydrochlorideHCID 76848196—
용매Acetic AcidHCID 176—
생성물5-bromo-2-(1,3-diethoxy-1,3-dioxopropan-2-yl)-6-fluoro-2,3,4,9-tetrahydro-1H-carbazole-8-carboxylic acidHCID 11776109049%

반응 단계

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)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09334290B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-9d6c9d1b33d246e588d4c05344625996
출처 메모uspto-grants-2016_05