HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1274145Erstellt: 26. Oktober 2026
Hydrazine → 3-Amino-6-chloro-5-hydrazino-pyrazine-2-carboxylic acid methyl ester
https://huagongshe.com/reaction/1274145
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrazine | HCID 9321 | — |
| Edukt | Methyl 3-amino-5,6-dichloropyrazine-2-carboxylate | HCID 73828 | — |
| Edukt | Dichloromethane methanol | HCID 21226129 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | tert-Butanol | HCID 6386 | — |
| Produkt | 3-Amino-6-chloro-5-hydrazino-pyrazine-2-carboxylic acid methyl ester | HCID 54167356 | — |
Reaktionsschritte
Methyl 3-amino-5,6-dichloro-2-pyrazinecarboxylate (1.10 g, 5 mmol) was dissolved in 20 mL of tert-butyl alcohol and DMF (v/v; 1:1). Anhydrous hydrazine (0.18 mL, 5.5 mmol) and N,N'-diisopropylethyl amine (4.5 mL, 25 mmol) were then added sequentially at 25° C. The resulting mixture was stirred at 25° C. for 12 h. The reaction mixture was then partitioned between EtOAc (100 mL) and sat. NaCl (aq) (100 mL). The organic layer was dried (Na2SO4), filtered, and concentrated in vacuo to give a brown solid residue. This residue was used in the next-step reaction without further purification: TLC (Rf =0.53; 10% MeOH/CH2Cl2).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06156758 |
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| Quelldatensatz | uspto-grants-2000_12 |
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| ORD ID | ord-3df39bd3e3f941c2a6a496870cdbcb92 |
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| Quellennotiz | uspto-grants-2000_12 |
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