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HRID 842763作成日:2026年10月26日

Acetic Acid → 5-[3,4-Dichlorophenoxy]-6-methoxy-8-[4-phthalimido-1-methyl-butylamino]lepidine

https://huagongshe.com/reaction/842763

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Sodium HydroxideHCID 14798—
反応物2-(4-Oxopentyl)-1H-isoindole-1,3(2H)-dioneHCID 236270—
反応物8-Amino-5-[3,4-dichlorophenoxy]-6-methoxylepidineHCID 609014—
反応物Sodium borohydrideHCID 4311764—
生成物5-[3,4-Dichlorophenoxy]-6-methoxy-8-[4-phthalimido-1-methyl-butylamino]lepidineHCID 633117—
生成物5-(3,4-Dichlorophenoxy)-6-methoxy-1methyl-8-[(4-phthalimido-1-methylbutyl)amino]quinolineHCID 69464197—

反応条件

温度30 °C

反応手順

A mixture of 12.4 g of 8-amino-5-(3,4-dichlorophenoxy)-6-methoxy-4-methylquinoline (36 mM) and 11.6 g of 4-oxo-1-phthalimidopentane (50 mM), in glacial acetic acid was stirred for 15 min under nitrogen and 2.6 g of sodium borohydride (70 mM) was added portionwise maintaining the temperature 25-35° C. After the addition, the reaction mixture was stirred for 30 min and then poured into ice cold solution of concentrated sodium hydroxide. The resulting precipitate was filtered and chromatographed over silica gel. Elution with hexanes:ethyl acetate 90:10 yielded the expected product of 5-(3,4-dichlorophenoxy)-6-methoxy-4-methyl-8-[(4-phthalimido-1-methylbutyl)amino]quino line which was crystallized from ether to give 12.4 g (22 mM) of yellow crystalline product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06376511B2
出典データセットuspto-grants-2002_04
ORD IDord-21095a23d393418fbcba0e1d862ca66b
出典メモuspto-grants-2002_04