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1,1-Dimethylhydrazine → [4-(Dimethyl-hydrazono)-piperidin-1-yl]-dimethyl-amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,1-Dimethylhydrazine | HCID 5976 | — |
| 反応物 | 1-(Dimethylamino)-4-piperidinone | HCID 56737782 | — |
| 生成物 | [4-(Dimethyl-hydrazono)-piperidin-1-yl]-dimethyl-amine | HCID 67227495 | 93.9% |
反応手順
3.0 g 1-Dimethylamino-piperidin-4-one (prepared as described in Journal of Medicinal & Pharmaceutical Chemistry, 4, 423-36; 1961) is cooled to 0° C., and 3.8 g N,N-dimethylhydrazine is added at such a rate, that the internal temperature does not exceed 15° C. The mixture is stirred at ambient temperature for 3 hours. Then the excess of N,N-dimethylhydrazine is evaporated. Thus, 3.65 g [4-(Dimethyl-hydrazono)-piperidin-1-yl]-dimethyl-amine is obtained. 1H-NMR (CDCl3): 2.80 ppm (m, 2H), 2.70 ppm (m, 4H), 2.45 ppm (s, 6H), 2.42 ppm (m, 2H), 2.40 ppm (s, 6H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08541343B2 |
| 出典データセット | uspto-grants-2013_09 |
| ORD ID | ord-7d02794213254b14860cca0a61ad4295 |
| 出典メモ | uspto-grants-2013_09 |