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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 636379Erstellt: 25. Oktober 2026

2,4-Difluorobenzoyl chloride → [2-Fluoro-4-(3-methyl-pyrazol-1-yl)-phenyl]-(11H-5-oxa-4,10-diaza-dibenzo[a,d]cyclohepten-10-yl)-methanone

https://huagongshe.com/reaction/636379

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,4-Difluorobenzoyl chlorideHCID 588081—
EduktSodiumHCID 5360545—
Edukt5,6-Dihydropyrido[2,3-b][1,5]benzoxazepineHCID 15895929—
Edukt(2,4-difluoro-phenyl)-(11H-5-oxa-4,10-diaza-dibenzo[a,d]cyclohepten-10-yl)-methanoneHCID 21254876—
EduktHCID 178428694HCID 178428694—
Produkt[2-Fluoro-4-(3-methyl-pyrazol-1-yl)-phenyl]-(11H-5-oxa-4,10-diaza-dibenzo[a,d]cyclohepten-10-yl)-methanoneHCID 9887219—

Reaktionsschritte

The title compound may be prepared in a manner analogous to that of the 2-chloro analog of Example 16, by reacting 6H-pyrido[2,3-b][1,5]benzoxazepine of Example 16, Step A with 2,4-difluoro benzoylchloride of Example 9, Step A. Subsequent reaction of the intermediate (2,4-difluoro-phenyl)-(11H-5-oxa-4,10-diaza-dibenzo[a,d]cyclohepten-10-yl)-methanone with the sodium salt of 3-methylpyrazole in a manner analogous to that of Example 16, Step C will provide the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06194407B1
Quelldatensatzuspto-grants-2001_02
ORD IDord-0ef0ea8a762a41a2ba2bda3c56c5322b
Quellennotizuspto-grants-2001_02