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Hydrazine hydrate (1:1) → 6-Chloro-3-hydrazinyl-4-methylpyridazine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrazine hydrate (1:1) | HCID 24654 | — |
| 反応物 | 3,6-Dichloro-4-methylpyridazine | HCID 87923 | — |
| 反応物 | 3-Hydrazinopyridazine | HCID 12295391 | — |
| 生成物 | 6-Chloro-3-hydrazinyl-4-methylpyridazine | HCID 11446490 | — |
| 生成物 | 3-Chloro-6-hydrazinyl-4-methylpyridazine | HCID 12376813 | — |
反応手順
The hydrazino pyridazine starting materials can be prepared by known procedures. For example, 3,6-dichloro-4-methylpyridazine heated at reflux with excess hydrazine hydrate (50 percent in water) for 0.3 to 1 hour produces 3-chloro-4-methyl-6-hydrazinopyridazine and 3-chloro-5-methyl-6-hydrazinopyridazine. The isomers can be separated by fractional crystallization using ethanol as a solvent. See, Takahayashi, Pharm. Bull., 5, 229 (1957); Chem. Abstr. 52:6359, Linholter et al., Acta Chem. Scand. 16, 2389 (1962); Chem. Abstr. 59:1632g, Steck et al., J. Amer. Chem. Soc., 76, 4454 (1954) and Horning et al., J. Org. Chem., 20, 707 (1955).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04526890 |
| 出典データセット | uspto-grants-1985_07 |
| ORD ID | ord-27363e9e87fb4363b9f1dfc5f6a295d9 |
| 出典メモ | uspto-grants-1985_07 |