HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 527322Erstellt: 25. Oktober 2026
Hydrazine hydrate (1:1) → 5-amino-3-((4-(methylsulfonyl)benzyl)amino)-1H-pyrazole-4-carboxamide
https://huagongshe.com/reaction/527322
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Edukt | 4-Methylsulfonylbenzylamine | HCID 57421 | — |
| Edukt | 2-Cyano-3,3-bis(methylthio)acrylamide | HCID 2747746 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 5-amino-3-((4-(methylsulfonyl)benzyl)amino)-1H-pyrazole-4-carboxamide | HCID 86701916 | — |
Reaktionsschritte
Dissolved 0.500 g 2-cyano-3,3-bis(methylthio)acrylamide in 15 mL EtOH and added 4-Methylsulphonylbenzylamine (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-(methylsulfonyl)benzyl)amino)-1H-pyrazole-4-carboxamide as a yellow powder. Product was allowed to dry under vacuum for 1 hr.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09346792B2 |
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| Quelldatensatz | uspto-grants-2016_05 |
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| ORD ID | ord-1b599d1dd5a243f58c1186066cf1d154 |
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| Quellennotiz | uspto-grants-2016_05 |
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