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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1269928Erstellt: 25. Oktober 2026

Cyanomethylenetributylphosphorane → HCID 178503317, Verbindung

https://huagongshe.com/reaction/1269928

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyanomethylenetributylphosphoraneHCID 4622928—
Edukt4-(methylthio)-1H-indazol-5-olHCID 22933648—
Edukttert-butyl 4-{[4-(methylsulfonyl)-1H-indazol-5-yl]oxy}azepane-1-carboxylateHCID 22933794—
EduktHCID 178515017HCID 178515017—
LösungsmittelTolueneHCID 1140—
ProduktHCID 178503317HCID 17850331758%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

The 4-(methylthio)-1H-indazol-5-ol (0.166 g, 0.92 mmol) obtained in Example 607 and the trans-2-(4-hydroxycyclohexyl)-1H-isoindole-1,3(2H)-dione (0.151 g, 0.61 mmol) obtained in Example 323, (a) were added to a solution of cyanomethylenetri-n-butylphosphorane (0.247 g, 0.92 mmol) in toluene (6 ml), and the resulting mixture was heated at 100° C. and stirred for 7 hours. The reaction solution was concentrated and then diluted with chloroform, and a 1N-aqueous sodium hydroxide solution was added thereto, followed by extraction with chloroform (three times). The extract solution was dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was purified by a silica gel chromatography (hexane/ethyl acetate=2/1˜1/1) to obtain 2-(cis-4-{[4-(methylthio)-1H-indazol-5-yl]oxy}cyclohexyl)-1H-isoindole-1,3(2H)-dione (0.144 g: 58%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07199147B2
Quelldatensatzuspto-grants-2007_04
ORD IDord-45618f7a7ec74444834daa30315ddd74
Quellennotizuspto-grants-2007_04