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HRID 527318作成日:2026年10月26日
Hydrazine hydrate (1:1) → 5-amino-3-((4-(4-methyl-1H-imidazol-1-yl)phenyl)amino)-1H-pyrazole-4-carboxamide
https://huagongshe.com/reaction/527318
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Hydrazine hydrate (1:1) | HCID 24654 | — |
| 反応物 | 2-Cyano-3,3-bis(methylthio)acrylamide | HCID 2747746 | — |
| 反応物 | 4-(4-Methyl-1h-imidazol-1-yl)benzenamine | HCID 16005170 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 5-amino-3-((4-(4-methyl-1H-imidazol-1-yl)phenyl)amino)-1H-pyrazole-4-carboxamide | HCID 86701914 | — |
反応手順
Dissolved 0.500 g 2-cyano-3,3-bis(methylthio)acrylamide in 15 mL EtOH and added 4-methyl-1-(4-aminophenyl)-1H-imidazole (1.0 eq.). Stirred reaction at 75° C. until starting amide was absent by HPLC. Once complete (18 hrs), reaction was brought to room temperature and filtered to obtain a light yellow powder as product. Product was allowed to dry under vacuum for 1 hr. Product was then suspended in 10 mL EtOH and hydrazine hydrate (1 eq.) was added dropwise. Reaction was heated at 75° C. until intermediate was absent (HPLC). Once intermediate was absent (18 hrs), reaction was brought to room temperature and filtered to obtain 5-amino-3-((4-(4-methyl-1H-imidazol-1-yl)phenyl)amino)-1H-pyrazole-4-carboxamide as a yellow powder. Product was allowed to dry under vacuum for 1 hr.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09346792B2 |
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| 出典データセット | uspto-grants-2016_05 |
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| ORD ID | ord-ad016818b21d49a28565f11af43437cf |
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| 出典メモ | uspto-grants-2016_05 |
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