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HRID 1808248作成日:2026年10月27日

Dimethylformamide → 4-Amino-3-fluoro-N-[2-(4-fluorophenoxy)-2-methylpropyl]benzamide

https://huagongshe.com/reaction/1808248

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物4-Amino-3-fluorobenzoic acidHCID 9971—
反応物DiisopropylethylamineHCID 81531—
反応物Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
反応物2-(4-Fluorophenoxy)-2-methylpropan-1-amineHCID 28917627—
生成物4-Amino-3-fluoro-N-[2-(4-fluorophenoxy)-2-methylpropyl]benzamideHCID 57732241—

反応手順

To a mixture of 4-amino-3-fluorobenzoic acid (200.0 mg, 1.289 mmol) and HBTU (490 mg, 1.3 mmol) in DMF (2 mL, 20 mmol) at 0° C. were added N,N-diisopropylethylamine (0.67 mL, 3.9 mmol) and 2-(4-fluorophenoxy)-2-methylpropan-1-amine (Preparation 91, 280 mg, 1.5 mmol). The reaction mixture was slowly warmed to ambient temperature. The reaction mixture was quenched with an equal volume of saturated aqueous sodium bicarbonate and extracted with ethyl acetate (3×). The combined organic layers were washed successively with water, aqueous lithium chloride, and brine, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified on the Isco (120 g cartridge, chloroform to 12% MeOH in chloroform).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08357711B2
出典データセットuspto-grants-2013_01
ORD IDord-a21d075e470f4516997390ef108200d2
出典メモuspto-grants-2013_01