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HRID 1945371作成日:2026年10月25日

Methyl 4-aminobenzoate → Methyl 4-({[4-(1-adamantyl)phenoxy]acetyl}amino)benzoate

https://huagongshe.com/reaction/1945371

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 4-aminobenzoateHCID 12082—
反応物DiisopropylethylamineHCID 81531—
反応物PMID26882240-Compound-8HCID 625381—
反応物Ethylcarbodiimide hydrochlorideHCID 21883477—
反応物HCID 178527226HCID 178527226—
溶媒DimethylformamideHCID 6228—
生成物Methyl 4-({[4-(1-adamantyl)phenoxy]acetyl}amino)benzoateHCID 347032151.7%

反応手順

To a mixture of [4-(1-adamantyl)phenoxy]acetic acid (143.2 mg, 0.5 mmol), 4-aminobenzoic acid methyl ester (113.4 mg, 0.5 mmol), N-3-dimethylaminopropyl)-N′-ethyl carbodiimide HCl (EDC) (143.8 mg, 0.75 mmol) and 1-hydroxybenzothiazole (HOBt) (101.4 mg, 0.75 mmol) in DMF (6 mL) was added N,N-diisopropylethylamine, redistilled (DIPEA) (97.0 mg, 0.13 mL, 0.75 mmol). The mixture was stirred overnight, and then partitioned between ethyl acetate and 10% HCl. The organic phase was washed with brine, dried (MgSO4 anh), and concentrated. The residue was purified by silica gel flash column chromatography (n-Hexane:Ethyl acetate:MeOH=6:3:1) to give 4-[2-(4-Adamantan-1-yl-phenoxy)-acetylamino]-benzoic acid methyl ester as a white solid (108.3 mg, 51.7% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08394799B2
出典データセットuspto-grants-2013_03
ORD IDord-5bb3175da738406fa5654c450b5e71e7
出典メモuspto-grants-2013_03