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HRID 1285134作成日:2026年10月27日

Potassium Carbonate → 1-(4-Fluorophenyl)-4-[4-(2-amino-3-nitro-pyridin-6-yl)-1-piperazinyl]-1-butanone ethylene ketal

https://huagongshe.com/reaction/1285134

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物6-Chloro-3-nitropyridin-2-ylamineHCID 2724035—
反応物1-(3-(2-(4-Fluorophenyl)-1,3-dioxolan-2-yl)propyl)piperazineHCID 2783121—
溶媒1-PropanolHCID 1031—
生成物1-(4-Fluorophenyl)-4-[4-(2-amino-3-nitro-pyridin-6-yl)-1-piperazinyl]-1-butanone ethylene ketalHCID 57145772—

反応手順

5.6 g 2-amino-6-chloro-3-nitropyridine, 10 g 1-(3-[2-(4-fluorophenyl)-1,3-dioxolan-2-yl]-propyl)piperazine, 5 g potassium carbonate and 100 ml n-propanol are refluxed 21/2 hours. After cooling the precipitate is filtered off. The filtrate is concentrated to ca. 10 ml and diluted with the same volume of diisopropyl ether. The resulting cristallisate is admixed with the above mentioned precipitate and partitioned between water and methylene chloride. The organic phase is filtered and evaporated to give the heading compound, m.p. 117°-118°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04565816
出典データセットuspto-grants-1986_01
ORD IDord-c37eaf3eae08407a8b0553640c833c89
出典メモuspto-grants-1986_01