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HRID 128143作成日:2026年10月26日

Ethylene Glycol → 2-Amino-5-(4-bromophenyl)-6-methylpyrazine

https://huagongshe.com/reaction/128143

反応式

関与物質

役割名称HCID仕込み量
反応物Ethylene GlycolHCID 174—
反応物2-Amino-3-carboxy-5-(4-bromophenyl)-6-methylpyrazineHCID 20567043—
溶媒TetralinHCID 8404—
溶媒Sodium HydroxideHCID 14798—
生成物2-Amino-5-(4-bromophenyl)-6-methylpyrazineHCID 12795610—

反応手順

Another intermediate pyrazine compound, 2-amino-5-(4-bromophenyl)-6-methylpyrazine is synthesized starting with 1-(4-bromophenyl)-1,2-propanedione 2-oxime, which oxime is obtained by the same general procedure of Hartung et al., supra. This oxime is allowed to react with aminomalononitrile tosylate, and the product, the substituted pyrazine 1-oxide, is allowed to react with phosphoruc trichloride in tetrahydrofuran, according to the procedure of Taylor et al., J. Org. Chem. 38, 2817 (1973), to yield 2-amino-3-cyano-5-(4-bromophenyl)-6-methylpyrazine. This product is then hydrolyzed in sodium hydroxide and ethylene glycol and the 2-amino-3-carboxy-5-(4-bromophenyl)-6-methylpyrazine so obtained is decarboxylated by heating in tetrahydronaphthalene to yield 2-amino-5-(4-bromophenyl)-6-methylpyrazine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号USRE030563
出典データセットuspto-grants-1981_03
ORD IDord-8926dc01d739424992b25cfa9d91e7a4
出典メモuspto-grants-1981_03