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Trimethylpyruvic acid → HCID 178441961、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Trimethylpyruvic acid | HCID 13150 | — |
| 反応物 | Thiocarbohydrazide | HCID 2724189 | — |
| 生成物 | HCID 178441961 | HCID 178441961 | — |
反応手順
which is formed in step (1) and which was hitherto unknown, is reacted, in a second stage, either directly in the solution obtained or after intermediate isolation and if appropriate after prior saponification to give free trimethylpyruvic acid (VI), with thiocarbohydrazide (H2N--NH--CS--NH--NH2) in an aqueous solution containing a hydrogen halide acid, at a temperature from about 20° to 100° C. in a manner which is in itself known to give 4-amino-6-tert.-butyl-3-mercapto-1,2,4-triazin-5(4H)-one (VII), and this compound is alkylated in alkaline solution, in a third stage, by means of methyl iodide or methyl bromide or other alkylating agents (especially ethyl iodide or ethyl bromide) in a known manner.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04309538 |
| 出典データセット | uspto-grants-1982_01 |
| ORD ID | ord-b7add5169a88451485b02245863f8ad2 |
| 出典メモ | uspto-grants-1982_01 |