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HRID 467作成日:2026年10月23日

1-Phenethylamine → 2-(alpha-Methylbenzylamino) pyrazine

https://huagongshe.com/ja/reaction/467

反応式

関与物質

役割名称HCID仕込み量
反応物1-PhenethylamineHCID 7408—
反応物ChloropyrazineHCID 73277—
試薬Sodium t-butoxideHCID 23676156—
触媒Binap, (A+-)-HCID 634876—
触媒Palladium (II) acetateHCID 4144353—
溶媒TolueneHCID 1140—
生成物2-(alpha-Methylbenzylamino) pyrazineHCID 2191934042.54%

反応条件

温度70 °C

反応手順

To a solution of 1-phenylethanamine (212 mg, 1.75 mmol) and 2-chloropyrazine (200 mg, 1.75 mmol) in toluene (10 mL) while bubbling N2 was added binap (141 mg, 0.23 mmol), sodium tert-butoxide (235 mg, 2.44 mmol) and palladium(II) acetate (51.0 mg, 0.23 mmol). The reaction mixure was heated at 70 oC for 3 hours. The reaction was concentrated, partitioned between ethyl acetate and water. The aqueous phase was extracted 3 times with ethyl acetate. The combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated. The crude material was loaded on a 40g silica gel column and purified on a Teledyne Isco instrument, eluting with 20% to 70% ethyl acetate in heptane to provide N-(1-phenylethyl)pyrazin-2-amine (148 mg, 42.5 %) as a solid.

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-74ae5f362208460ebf2f7ad1b936b06b
出典メモ750 AstraZeneca ELN dataset