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HRID 27789作成日:2026年10月27日

8-Hydroxy-5-(1-hydroxy-2-((1-methylethyl)amino)butyl)-2(1H)-quinolinone → 5-(1-Hydroxy-2-isopropylaminobutyl)-8-isobutyryloxycarbostyril hydrochloride

https://huagongshe.com/reaction/27789

反応式

関与物質

役割名称HCID仕込み量
反応物8-Hydroxy-5-(1-hydroxy-2-((1-methylethyl)amino)butyl)-2(1H)-quinolinoneHCID 4916—
反応物ChloroformHCID 6212—
反応物Isobutyric anhydrideHCID 7346—
生成物5-(1-Hydroxy-2-isopropylaminobutyl)-8-isobutyryloxycarbostyril hydrochlorideHCID 23342055—
生成物2,8-Diisobutyryloxy-5-(1-hydroxy-2-isopropylaminobutyl)quinoline hydrochlorideHCID 23342072—
生成物2-Isobutyryloxy-5-(1-hydroxy-2-isopropylaminobutyl)-8-hydroxyquinoline hydrochlorideHCID 23342073—
生成物5-(1-Isobutyryloxy-2-isopropylaminobutyl)-8-isobutyryloxycarbostyril hydrochloride monohydrateHCID 23342090—

反応手順

3 g of 5-(1-hydroxy-2-isopropylaminobutyl)-8-hydroxycarbostyril was added to 200 ml of anhydrous chloroform, and 3 ml of isobutyric anhydride was added dropwise to the mixture. The resulting mixture was stirred for 5 hours at room temperature, and the solvent was removed by distillation under reduced pressure. Petroleum ether was added to the residue, and the crystals formed were separated by filtration. The crystals were rendered neutral with 50 ml of a cold saturated aqueous solution of sodium bicarbonate, and insoluble material was separated by filtration and washed with water. The resulting material which was found to be a mixture of about 7 components by thin layer chromatography was then subjected to silica gel column chromatography using a silica gel of Grade C-200 (trade name of Wako Junyaku, Japan) and a mixture of chloroform and methanol (20:1 by volume) as an eluant to obtain an eluate containing four main components. The solvent was then removed by distillation from the eluate, and 5 ml of a saturated ethanolic solution of hydrogen chloride was added to the residue. Petroleum ether was added to the mixture, and the precipitated crystals were separated by filtration and recrystallized from acetone to obtain, as main components, 1.5 g of 5-(1-isobutyryloxy-2-isopropylaminobutyl)-8-isobutyryloxycarbostyril hydrochloride monohydrate having a melting point of 198°-199° C., 0.1 g of 2,8-diisobutyryloxy-5-(1-hydroxy-2-isopropylaminobutyl)quinoline hydrochloride having a melting point of 201°-203° C. (with decomposition), 0.4 g of 5-(1-hydroxy-2 -isopropylaminobutyl)-8-isobutyryloxycarbostyril hydrochloride having a melting point of 228°-229° C. (with coloration and decomposition), and 0.1 g of 2-isobutyryloxy-5-(1-hydroxy-2-isopropylaminobutyl)-8-hydroxyquinoline hydrochloride having a melting point of 225°-226.5° C. (with coloration and decomposition).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04223137
出典データセットuspto-grants-1980_09
ORD IDord-a2b56df9f42744e783aae64bb239f7cd
出典メモuspto-grants-1980_09