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HRID 2406714作成日:2026年10月25日

Tetrahydrofuran → 4-(3-Bromo-5-nitropyridin-2-yl)morpholine

https://huagongshe.com/reaction/2406714

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物MorpholineHCID 8083—
反応物TriethylamineHCID 8471—
反応物3-Bromo-2-chloro-5-nitropyridineHCID 230889—
溶媒WaterHCID 962—
生成物4-(3-Bromo-5-nitropyridin-2-yl)morpholineHCID 4673888095.1%

反応手順

Triethylamine (191 mg) and morpholine (120 mg) were added to a tetrahydrofuran (4 ml) solution containing 3-bromo-2-chloro-5-nitropyridine (300 mg), followed by stirring for 40 minutes. Water was added to the reaction solution, followed by extraction with ethyl acetate. The resultant was washed with saturated saline and dried over anhydrous sodium sulfate. Subsequently, the solvent was distilled away under reduced pressure, the obtained residue was purified by silica gel chromatography (chloroform:methanol=1:0 to 3:1), and a yellow solid of 4-(3-bromo-5-nitropyridin-2-yl)morpholine (346 mg) was thus obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08809371B2
出典データセットuspto-grants-2014_08
ORD IDord-cae4fa630e6f466b8d9745dd238dabe9
出典メモuspto-grants-2014_08