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HRID 2094569Erstellt: 25. Oktober 2026

Diethyl Ether → 3-(4-Chloro-6-morpholin-4-yl-[1,3,5]triazin-2-yloxy)-8-methyl-8-azabicyclo[3.2.1]octane

https://huagongshe.com/reaction/2094569

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
Edukt8-Methyl-8-azabicyclo(3.2.1)octan-3-olHCID 8424—
Edukt2,4-Dichloro-6-morpholino-1,3,5-triazineHCID 81076—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-(4-Chloro-6-morpholin-4-yl-[1,3,5]triazin-2-yloxy)-8-methyl-8-azabicyclo[3.2.1]octaneHCID 8723960742%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

In a three neck flask equipped with stirring bar under N2 atmosphere tropine (1 g, 4.24 mmol) was suspended in (anhydrous) THF (15 mL). The mixture was cooled to −78° C. and BuLi (2M in THF) (5.53 ml, 1.2 eq) was added dropwise and the mixture was allowed to warm to 25° C. over 30 minutes. To the reaction mixture 2,4,-dichloro-6-morpholin-4-yl-[1,3,5]triazine (996 mg, 4,24, mmole) was added and allowed to stir overnight. For work up, ether (100 mL) was added. The organic layer was washed with water (20 mL) and brine (20 mL) and dried over MgSO4. filtered and the solvents were removed to obtain a colorless oil. Further purification by flash-chromatography using CH2Cl2/MeOH/NH3 (15:1:0.1) gave the product as white solid (600 mg, 42% yield); MS (ESI) m/z 340

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08445486B2
Quelldatensatzuspto-grants-2013_05
ORD IDord-1038fdff418244c5901cae86f6bc11a9
Quellennotizuspto-grants-2013_05