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HRID 353596作成日:2026年10月26日

Acetic Acid → (2-(4-((6-Quinolylamino)methyl)phenoxy)ethyl)diethylamine

https://huagongshe.com/reaction/353596

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物6-AminoquinolineHCID 11373—
反応物Sodium HydroxideHCID 14798—
反応物4-(2-(Diethylamino)-Ethoxy)-BenzaldehydeHCID 411674—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒1,2-DichloroethaneHCID 11—
生成物(2-(4-((6-Quinolylamino)methyl)phenoxy)ethyl)diethylamineHCID 235143838.3%

反応手順

To a stirred solution of 1.0 gram (0.0045 mole) of 4-(2-(diethylamino)ethoxy)benzaldehyde and 0.65 gram (0.0045 mole) of 6-aminoquinoline (available from Aldrich Chemical Company) in 25 mL of 1,2-dichloroethane (DCE, available from Aldrich Chemical Company) was added 0.3 mL (0.0045 mole) of glacial acetic acid (available from J. T. Baker Inc.) followed by 1.4 grams (0.0068 mole) of sodium triacetoxyborohydride (available from Aldrich Chemical Company). Upon completion of addition, the reaction mixture was stirred at ambient temperature for three hours. At the conclusion of this period, 50 mL of 10% aqueous sodium hydroxide was added dropwise. The resulting solution was extracted with three 25 mL portions of diethyl ether. The extracts were combined, washed with one 25 mL portion of an aqueous solution saturated with sodium chloride, dried with sodium sulfate and filtered. The filtrate was concentrated under reduced pressure, yielding 1.25 grams of a dark brown paste. The dark brown paste was purified by column chromatography on silica gel, yielding 0.13 gram of Compound 15. The NMR spectrum was consistent with the proposed structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06753429B2
出典データセットuspto-grants-2004_06
ORD IDord-fcbe1e5a9d5b42bea75a6652b652f34a
出典メモuspto-grants-2004_06