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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 128143생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/128143

반응식

참여 물질

역할이름HCID투입량
반응물Ethylene GlycolHCID 174—
반응물2-Amino-3-carboxy-5-(4-bromophenyl)-6-methylpyrazineHCID 20567043—
용매TetralinHCID 8404—
용매Sodium HydroxideHCID 14798—
생성물2-Amino-5-(4-bromophenyl)-6-methylpyrazineHCID 12795610—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE030563
출처 데이터셋uspto-grants-1981_03
ORD IDord-8926dc01d739424992b25cfa9d91e7a4
출처 메모uspto-grants-1981_03