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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1434132Erstellt: 25. Oktober 2026

8-Methyl-8-azabicyclo(3.2.1)octan-3-ol → HCID 58023090, Verbindung

https://huagongshe.com/reaction/1434132

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt8-Methyl-8-azabicyclo(3.2.1)octan-3-olHCID 8424—
EduktSodium hydrideHCID 24758—
EduktSodium BicarbonateHCID 516892—
Edukt3,4-Difluorobenzoyl chlorideHCID 2724519—
EduktEthyl[5-methoxy-2-(6-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)phenyl]amineHCID 23087318—
EduktN-ethyl-3,4-difluoro-N-[5-methoxy-2-(6-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)phenyl]benzamideHCID 66627253—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 58023090HCID 5802309029,4%

Reaktionsschritte

To a suspension of 60% sodium hydride (187 mg) in N,N-dimethylformamide (2 ml) was added tropine (599 mg) on an ice bath. The solution was stirred for 30 minutes while warming to room temperature. Synthesized from ethyl [5-methoxy-2-(6-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)phenyl]amine and 3,4-difluorobenzoyl chloride according to an analogous synthetic method to Preparation Example 87, a solution of N-ethyl-3,4-difluoro-N-[5-methoxy-2-(6-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)phenyl]benzamide (383 mg) in N,N-dimethylformamide (5 ml) was added the above solution followed by stirring overnight at 80° C. The reaction mixture was let to cool, then a saturated aqueous solution of sodium bicarbonate was added thereto, the solution was extracted with ethyl acetate, then sequentially washed with water and brine, dried over anhydrous potassium carbonate, and then the solvent was evaporated in vacuo. The residue was purified by NH silica gel column chromatography (chloroform-methanol system) to provide the title compound (143 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07612114B2
Quelldatensatzuspto-grants-2009_11
ORD IDord-283bbe4ff9b0437183cf77bc83225d1d
Quellennotizuspto-grants-2009_11