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HRID 1431152Erstellt: 27. Oktober 2026

6-Amino-3-chloropyridazine → 6-((1S,4S)-5-Methyl-2,5-diaza-bicyclo[2.2.1]hept-2-yl)-pyridazin-3-ylamine

https://huagongshe.com/reaction/1431152

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt6-Amino-3-chloropyridazineHCID 21643—
Edukt(1S,4S)-2-Methyl-2,5-diazabicyclo[2.2.1]heptaneHCID 11029795—
LösungsmittelDichloromethaneHCID 6344—
Produkt6-((1S,4S)-5-Methyl-2,5-diaza-bicyclo[2.2.1]hept-2-yl)-pyridazin-3-ylamineHCID 66743079—

Reaktionsbedingungen

Temperatur200 °C

Reaktionsschritte

6-Chloropyridazin-3-amine (200 mg, 1.54 mmol, Eq: 1.00) and (1S,4S)-2-methyl-2,5-diazabicyclo[2.2.1]heptane (693 mg, 6.18 mmol, Eq: 4.00) were combined in a small round bottom flask and heated at 200° C. for 2 hours. The dark glassy residue was dissolved in DCM and purified by chromatography using a gradient of 0% to 25% methanol (with 2.5% ammonium hydroxide) in DCM to give about 100 mg (31.6%) of a brown, viscous oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08940741B2
Quelldatensatzuspto-grants-2015_01
ORD IDord-02d80ceeed7b4968b338a47a688e8aed
Quellennotizuspto-grants-2015_01