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HRID 489745作成日:2026年10月25日

Methylamine → (2R)-(4E)-N-Methyl-5-(3-pyridyl)-4-penten-2-amine

https://huagongshe.com/reaction/489745

反応式

関与物質

役割名称HCID仕込み量
反応物MethylamineHCID 6329—
反応物(2S)-(4E)-5-(3-pyridyl)-4-penten-2-ol p-toluenesulfonateHCID 87465994—
生成物(2R)-(4E)-N-Methyl-5-(3-pyridyl)-4-penten-2-amineHCID 9898976—

反応条件

温度105 °C

反応手順

A mixture of (2S)-(4E)-5-(3-pyridyl)-4-penten-2-ol p-toluenesulfonate (3.80 g, 11.97 mmol) and methylamine (20 mL, 2.0M solution in THF) was heated at 100-110° C. for 8 h in a sealed glass tube. The mixture was cooled to ambient temperature and concentrated under reduced pressure on a rotary evaporator. The resulting brown syrup was diluted with saturated NaHCO3 solution (25 mL) and extracted with chloroform (4×25 mL). The combined chloroform extracts were dried (K2CO3), filtered, and concentrated by rotary evaporation to afford a thick, brown syrup (2.00 g). The crude product was purified by column chromatography on silica gel, eluting with chloroform-methanol (95:5, v/v). Selected fractions were combined, concentrated by rotary evaporation affording a 800 mg (37.9%) of a pale-yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06979695B2
出典データセットuspto-grants-2005_12
ORD IDord-c1f47da3d71b446ca9c2f525bf45ecc5
出典メモuspto-grants-2005_12