참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethylene Glycol | HCID 174 | — |
| 반응물 | 2-Amino-3-carboxy-5-(4-bromophenyl)-6-methylpyrazine | HCID 20567043 | — |
| 용매 | Tetralin | HCID 8404 | — |
| 용매 | Sodium Hydroxide | HCID 14798 | — |
| 생성물 | 2-Amino-5-(4-bromophenyl)-6-methylpyrazine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | USRE030563 |
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| 출처 데이터셋 | uspto-grants-1981_03 |
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| ORD ID | ord-8926dc01d739424992b25cfa9d91e7a4 |
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| 출처 메모 | uspto-grants-1981_03 |
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