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(2,4,6-Trichlorophenyl)hydrazine → 5-Cyano-6-methyl-1-(2,4,6-trichloroanilino)-2,4-pyrimidinedione
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | (2,4,6-Trichlorophenyl)hydrazine | HCID 79234 | — |
| 反応物 | alpha-cyano-beta-methyl-beta-(2,4,6-trichlorophenylhydrazino)-N-ethoxycarbonylacrylamide | HCID 70513266 | — |
| 生成物 | 5-Cyano-6-methyl-1-(2,4,6-trichloroanilino)-2,4-pyrimidinedione | HCID 13232255 | — |
反応手順
Following the method of Example 1, N-ethoxycarbonylcyanoacetamide is heated with triethyl orthoacetate and acetic anhydride to give α-cyano-β-ethoxy-β-methyl-N-ethoxycarbonylacrylamide, which in turn is reacted with 2,4,6-trichlorophenylhydrazine. The resulting compound α-cyano-β-methyl-β-(2,4,6-trichlorophenylhydrazino)-N-ethoxycarbonylacrylamide (m.p.=183°-184°) is cyclized, yielding 5-cyano-6-methyl-1-(2,4,6-trichloroanilino)-2,4-pyrimidinedione, m.p.=>305°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04411839 |
| 出典データセット | uspto-grants-1983_10 |
| ORD ID | ord-aebfeb5fb5064674a31c808ff9acdc9b |
| 出典メモ | uspto-grants-1983_10 |