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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrazineHCID 9321—
EduktMethyl 3-amino-5,6-dichloropyrazine-2-carboxylateHCID 73828—
EduktDichloromethane methanolHCID 21226129—
LösungsmittelDimethylformamideHCID 6228—
Lösungsmitteltert-ButanolHCID 6386—
Produkt3-Amino-6-chloro-5-hydrazino-pyrazine-2-carboxylic acid methyl esterHCID 54167356—

Reaktionsbedingungen

Temperatur25 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06156758
Quelldatensatzuspto-grants-2000_12
ORD IDord-3df39bd3e3f941c2a6a496870cdbcb92
Quellennotizuspto-grants-2000_12