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5-Hydroxy-4,4-dimethyl-1-pentanesulfonamide → 1-Pentanesulfonamide, 4,4-dimethyl-5-((7-methyl(1,2,4)triazolo(1,5-b)pyridazin-6-yl)oxy)-
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 5-Hydroxy-4,4-dimethyl-1-pentanesulfonamide | HCID 10726520 | — |
| 反応物 | 6-Chloro-7-methyl-[1,2,4]triazolo[1,5-b]pyridazine | HCID 11805158 | — |
| 生成物 | 1-Pentanesulfonamide, 4,4-dimethyl-5-((7-methyl(1,2,4)triazolo(1,5-b)pyridazin-6-yl)oxy)- | HCID 3073788 | — |
反応手順
Using 5-hydroxy-4,4-dimethyl-1-pentanesulfonamide and 6-chloro-7-methyl[1,2,4]triazolo[1,5-b]pyridazine, the same reaction was conducted as in Example 5 to produce the title compound. m.p. 171°-172° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05389633 |
| 出典データセット | uspto-grants-1995_02 |
| ORD ID | ord-55d85fa45f36489eabca2860c9c974a7 |
| 出典メモ | uspto-grants-1995_02 |