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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2359811Erstellt: 27. Oktober 2026

Water → 3-[Bis(tert-butoxycarbonyl)aminomethyl]-6-phenylpyridazine

https://huagongshe.com/reaction/2359811

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktPotassium CarbonateHCID 11430—
EduktDi-tert-butyl IminodicarboxylateHCID 279800—
Edukt3-(Bromomethyl)-6-phenylpyridazineHCID 66717445—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-[Bis(tert-butoxycarbonyl)aminomethyl]-6-phenylpyridazineHCID 6671770097%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

To a solution of 3-bromomethyl-6-phenylpyridazine (120 mg, 0.482 mmol) obtained in Reference Example 2-(a) in N,N-dimethylformamide (1.57 ml) were added di-tert-butyl iminodicarboxylate (127 mg, 0.585 mmol) and potassium carbonate (134 mg, 0.970 mmol), followed by stirring at 50° C. for 2 hours. After completion of the reaction, water was added to the reaction solution, followed by extraction with ethyl acetate. The separated organic layer was dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography (eluent; hexane:ethyl acetate=2:1→1:1 (V/V)), and fractions containing the desired compound were concentrated under reduced pressure to afford the title compound (180 mg) as a slightly yellow solid. (Yield: 97%)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08685986B2
Quelldatensatzuspto-grants-2014_04
ORD IDord-758a4a0eba134c9d8bef620388914d09
Quellennotizuspto-grants-2014_04