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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1253758Erstellt: 26. Oktober 2026

Sodium hydride → 9-(Pyridin-4-yl-methyl)-3,9-diazaspiro[5.5]undecane-3-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1253758

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
Edukttert-Butyl 3,9-diazaspiro[5.5]undecane-3-carboxylateHCID 15296367—
Edukt4-(Bromomethyl)pyridine hydrochlorideHCID 22274151—
LösungsmittelDimethylformamideHCID 6228—
Produkt9-(Pyridin-4-yl-methyl)-3,9-diazaspiro[5.5]undecane-3-carboxylic acid tert-butyl esterHCID 5950554635%

Reaktionsschritte

NaH (60% strength in mineral oil, 709 mg, 29.52 mmol) was added to a mixture of 3,9-diazaspiro[5.5]undecane-3-carboxylic acid tert-butyl ester (2.5 g, 9.84 mmol) in DMF (50 ml) at 0° C., the mixture was stirred at room temperature for 2 h, 4-(bromomethyl)-pyridine HCl (2.42 mg, 14.76 mmol) was then added and the mixture was stirred at room temperature for 16 h. Finally, ice was added and the reaction mixture was extracted with ethyl acetate. The combined organic phases were washed with water and sat. NaCl solution, dried over sodium sulfate and concentrated under reduced pressure. The crude product was purified by column chromatography (mobile phase methanol/methylene chloride). Yield: 35%

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08455475B2
Quelldatensatzuspto-grants-2013_06
ORD IDord-8a02c1fad1c04ce89971ad086e548559
Quellennotizuspto-grants-2013_06