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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2301838Erstellt: 25. Oktober 2026

5-(tert-butyldimethylsilyloxy)-2-phthalimido-N-[[1-(4-pyridyl)piperidin-4-yl]methoxycarbonyl]aniline → 4-(tert-Butyldimethyl-silyloxy)-N2-[1-(4-pyridyl)piperidin-4-yl]methoxycarbonyl-1,2-benzenediamine

https://huagongshe.com/reaction/2301838

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-(tert-butyldimethylsilyloxy)-2-phthalimido-N-[[1-(4-pyridyl)piperidin-4-yl]methoxycarbonyl]anilineHCID 18174529—
LösungsmittelMethanolHCID 887—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelHydrazineHCID 9321—
Produkt4-(tert-Butyldimethyl-silyloxy)-N2-[1-(4-pyridyl)piperidin-4-yl]methoxycarbonyl-1,2-benzenediamineHCID 5386097186%

Reaktionsschritte

A solution of 5-(tert-butyldimethylsilyloxy)-2-phthalimido-N-[[1-(4-pyridyl)piperidin-4-yl]methoxycarbonyl]aniline (1.34 g, 2.28 mmol) in 1 M hydrazine in methanol (6 mL) was stirred at ambient temperature for 40 h during which time a white precipitate formed. The mixture was further diluted with methylene chloride and cooled with an ice bath then filtered. The filtrate was washed once with saturated sodium chloride solution, dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo to yield 890 mg (86%) of the title compound as a tan powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06500851B2
Quelldatensatzuspto-grants-2002_12
ORD IDord-f907f14439004aa5a9f5d305fa44bc13
Quellennotizuspto-grants-2002_12