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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 249750Erstellt: 25. Oktober 2026

Sodium Hydroxide → HCID 16005059, Verbindung

https://huagongshe.com/reaction/249750

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
EduktN,N-Dimethyl-1H-imidazole-1-sulfonamideHCID 395751—
Edukt5-(2-Bromopyrid-5-yl)-1-azabicyclo[3.2.1]octaneHCID 86259378—
EduktButyllithiumHCID 178418339—
KatalysatorZincchlorideHCID 3007855—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelChloroformHCID 6212—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
ProduktHCID 16005059HCID 16005059—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

1 g (5.7 mmol) of 1-(dimethylaminosulfonyl)imidazole dissolved in 9 ml of tetrahydrofuran is introduced into a 25 ml three-necked flask. The reaction medium is cooled to −78° C. and 4 ml of a 1.6M solution of n-butyllithium in hexane is added dropwise over 20 minutes. 0.73 g (5.4 mmol) of zinc chloride dissolved in 4 ml of tetrahydrofuran is then added. The mixture is stirred while allowing the temperature to return to 20° C., and 1.5 g (11.1 mmol) of zinc chloride, 0.1 g (0.09 mmol) of tetrakis(triphenylphosphine)palladium and 0.56 g (2.1 mmol) of (−)-5-(2-bromopyrid-5-yl)-1-azabicyclo[3.2.1]octane (prepared according to the method described in step 1.2 of Example 1), dissolved in 5 ml of tetrahydrofuran, are then successively added. The mixture is then refluxed for 24 hours and then cooled to room temperature. 30 ml of aqueous 30% sodium hydroxide solution and 50 ml of chloroform are added. The aqueous phase is extracted with chloroform and the combined organic phases are then washed with saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered and concentrated under reduced pressure. The residue is purified by chromatography on a column of silica gel, eluting with a mixture of chloroform, methanol and aqueous ammonia in 95/5/0.5 proportions and is used in the following step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07863290B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-e51c26fb3ced42af8c861c6ce33ba6ab
Quellennotizuspto-grants-2011_01