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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 602005Erstellt: 23. Oktober 2026

Ammonium Chloride → N-(2-chlorocyclohexyl)-3,5-difluoro-4-(2-propynyloxy)benzamide

https://huagongshe.com/de/reaction/602005

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
Edukt7-[3,5-Difluoro-4-(2-propynyloxy)benzoyl]-7-azabicyclo[4.1.0]heptaneHCID 57701178—
KatalysatorZincchlorideHCID 3007855—
LösungsmittelChloroformHCID 6212—
ProduktN-(2-chlorocyclohexyl)-3,5-difluoro-4-(2-propynyloxy)benzamideHCID 57701136—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

A mixture of 4 ml of chloroform and 298 mg of zinc (II) chloride was stirred at 60° C. After 5 minutes, a mixture of 291 mg of 7-[3,5-difluoro-4-(2-propynyloxy)benzoyl]-7-azabicyclo[4.1.0]heptane and 2 ml of chloroform was added dropwise thereto at 60° C., and the resulting mixture was heated under reflux for 5 hours. Then, an aqueous saturated ammonium chloride solution was added to the reaction mixture, and this was extracted with chloroform. The organic layer was dried over magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 0.22 g of N-(2-chlorocyclohexyl)-3,5-difluoro-4-(2-propynyloxy)benzamide (hereinafter, described as the compound 87 of the present invention) represented by the formula:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07902400B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-9c87c08183054d25addd37cb2ab63ce0
Quellennotizuspto-grants-2011_03