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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1788979생성일: 2026년 10월 26일

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

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TriethylamineHCID 8471—
반응물1-Ethyl-6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acidHCID 9835179—
반응물Piperazin-1-ol dihydrochlorideHCID 12463394—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물1-Ethyl-6,8-difluoro-1,4-dihydro-7-(4-hydroxypiperazin-1-yl)-4-oxoquinoline-3-carboxylic acidHCID 306584881.1%

반응 조건

온도100 °C

반응 단계

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.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04686221
출처 데이터셋uspto-grants-1987_08
ORD IDord-69a2a105fbf243efb1c35a56bb089878
출처 메모uspto-grants-1987_08