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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2301837Erstellt: 25. Oktober 2026

Phosgene → 5-(tert-butyldimethylsilyloxy)-2-phthalimido-N-[[1-(4-pyridyl)piperidin-4-yl]methoxycarbonyl]aniline

https://huagongshe.com/reaction/2301837

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhosgeneHCID 6371—
Edukt(1-(Pyridin-4-YL)piperidin-4-YL)methanolHCID 11310048—
Edukt5-(Tert-butyldimethylsilyloxy)-2-phthalimidoanilineHCID 18174494—
LösungsmittelTolueneHCID 1140—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelHexaneHCID 8058—
Produkt5-(tert-butyldimethylsilyloxy)-2-phthalimido-N-[[1-(4-pyridyl)piperidin-4-yl]methoxycarbonyl]anilineHCID 1817452990%

Reaktionsschritte

A solution of 5-(tert-butyldimethylsilyloxy)-2-phthalimidoaniline (1.02 g, 2.77 mmol) in toluene (15 mL) was treated with a solution of 20% phosgene in toluene (2 mL) at reflux for 20 min. The volatile materials were removed in vacuo to give a tan solid, which was dissolved in dry methylene chloride (20 mL) and treated with 1-(4-pyridyl)piperidine-4-methanol (0.53 g, 2.77 mmol). The resulting suspension was stirred for 90 min then diluted with hexane. The mixture was allowed to stand overnight and the resulting precipitate collected by vacuum filtration and dried to yield 1.46 g (90%) of the title compound as a tan powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06500851B2
Quelldatensatzuspto-grants-2002_12
ORD IDord-205459866a12411891d4752ff126a896
Quellennotizuspto-grants-2002_12