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HRID 1788979作成日:2026年10月27日

Hydrochloric Acid → 1-Ethyl-6,8-difluoro-1,4-dihydro-7-(4-hydroxypiperazin-1-yl)-4-oxoquinoline-3-carboxylic acid

https://huagongshe.com/reaction/1788979

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物TriethylamineHCID 8471—
反応物1-Ethyl-6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acidHCID 9835179—
反応物Piperazin-1-ol dihydrochlorideHCID 12463394—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
生成物1-Ethyl-6,8-difluoro-1,4-dihydro-7-(4-hydroxypiperazin-1-yl)-4-oxoquinoline-3-carboxylic acidHCID 306584881.1%

反応条件

温度100 °C

反応手順

1-Hydroxypiperazine dihydrochloride (3.94 g) (which is prepared in Preparation 1), triethylamine (21 ml) and dimethylsulfoxide (30 ml) are added to 1-ethyl-6,7,8-trifluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid (4.07 g), which is prepared according to the procedure described in Japanese Patent First Publication No. 30964/1981, and the mixture is heated at 100° C. for 30 minutes. After cooling to room temperature, water (200 ml) is added to the mixture and the pH is adjusted to 7.0 with dil. HCl. The precipitated crystals are filtered, washed with water and dried. The product is recrystallized from a mixture of dimethylformamide and water to yield 1-ethyl-6,8-difluoro-1,4-dihydro-7-(4-hydroxypiperazin-1-yl)-4-oxoquinoline-3-carboxylic acid (4.3 g) as pale yellow needles, m.p. 253°-260° C. (decomposed with foaming) (which starts to color brown at around 234° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04686221
出典データセットuspto-grants-1987_08
ORD IDord-69a2a105fbf243efb1c35a56bb089878
出典メモuspto-grants-1987_08