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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1107753Erstellt: 26. Oktober 2026

2,4-Difluorobenzyl alcohol → 1-(2-Butenyl)-7-(2,4-difluorobenzyloxy)-2,3-dimethylpyrrolo[2,3-d]pyridazine

https://huagongshe.com/reaction/1107753

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,4-Difluorobenzyl alcoholHCID 91867—
Edukt1-(2-Butenyl)-7-chloro-2,3-dimethylpyrrolo[2,3-d]pyridazineHCID 53719624—
Produkt1-(2-Butenyl)-7-(2,4-difluorobenzyloxy)-2,3-dimethylpyrrolo[2,3-d]pyridazineHCID 5391037443,1%

Reaktionsschritte

The title compound (cis/trans=18/82) was prepared as a pale yellow powder in 43.1% yield in a similar procedure to that described in Example 1 by using 1-(2-butenyl)-7-chloro-2,3-dimethylpyrrolo[2,3-d]pyridazine (cis/trans=21/79) and 2,4-difluorobenzyl alcohol.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06063782
Quelldatensatzuspto-grants-2000_05
ORD IDord-5028f0128512400995d3b0e575ddb826
Quellennotizuspto-grants-2000_05