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HRID 1184323作成日:2026年10月26日

4-(5-Amino-6-(phenylmethyl)-2-pyrazinyl)phenol → 2-((3-Benzyl-5-(4-hydroxyphenyl)pyrazin-2-yl)amino)hexanoic acid

https://huagongshe.com/reaction/1184323

反応式

関与物質

役割名称HCID仕込み量
反応物4-(5-Amino-6-(phenylmethyl)-2-pyrazinyl)phenolHCID 193743—
反応物2-ketohexanoic acid sodium saltHCID 23669158—
触媒Acetic AcidHCID 176—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物2-((3-Benzyl-5-(4-hydroxyphenyl)pyrazin-2-yl)amino)hexanoic acidHCID 13639103446.1%

反応条件

温度65 °C

反応手順

4-(5-amino-6-benzylpyrazin-2-yl)phenol (200 mg, 0.72 mmol) was mixed with 2-Ketohexanoic acid sodium salt (220 mg, 1.44 mmol) in ethanol (20 mL). Pd/C (10% Palladium in active carbon, 100 mg) was added with a few drops of acetic acid, and the reaction mixture heated to 65° C. Air was bubbled out by N2 gas, and a hydrogen balloon applied to the reaction flask. The reaction was continuously stirred for 4 hrs. After cooling down, it was filtered and the resulting solution was purified by flash chromatography (eluting solvent: 50% EtOAc in heptanes) to give the product as a yellow powder (130 mg, 46%). MS (ESI): m/z 392.2 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08669103B2
出典データセットuspto-grants-2014_03
ORD IDord-09c14d7b97c74c56842601b59e24e20a
出典メモuspto-grants-2014_03