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HRID 1461712作成日:2026年10月25日

Potassium Iodide → 1-Cyclopropyl-7-[4-(diethoxyphosphinyl)-1-piperazinyl]-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic Acid, 2-Methoxyethyl Ester

https://huagongshe.com/reaction/1461712

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Cesium carbonateHCID 10796—
反応物Potassium HydroxideHCID 14797—
反応物2-Bromoethyl methyl etherHCID 80972—
反応物1-Cyclopropyl-7-[4-(diethoxyphosphinyl)-1-piperazinyl]-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic AcidHCID 15028007—
溶媒Diethyl EtherHCID 3283—
溶媒HexamethylphosphoramideHCID 12679—
生成物1-Cyclopropyl-7-[4-(diethoxyphosphinyl)-1-piperazinyl]-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic Acid, 2-Methoxyethyl EsterHCID 1502801580.8%

反応手順

To a solution of 0.467 g of the product of Example 40 in 5 ml of hexamethylphosphoramide was added 0.163 g of cesium carbonate, 0.304 g of 2-bromoethyl methyl ether, 0.137 g of 45% aqueous potassium hydroxide and 0.017 g of potassium iodide. The suspension was stirred in the dark under argon for 8 days. Ether (40 ml) was added and the mixture was extracted successively with water, brine and water. The ether layer was discarded. The aqueous layers were extracted with chloroform, the chloroform extracts were dried over sodium sulfate and then evaporated, finally at <100° and 0.06 mm. to remove hexamethylphosphoramide. Two recrystallizations of the solid residue from methylene chloride-n-heptane gave 0.424 g of ivory-colored needles, m.p. 138°-141° C. The product was easily soluble in water and in 0.1 M phosphate buffer, pH 7.5.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05077282
出典データセットuspto-grants-1991_12
ORD IDord-b5b7ef62c2b4466c8b811f1b82f26a13
出典メモuspto-grants-1991_12