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HRID 1778468Erstellt: 25. Oktober 2026

Isopropyl iodide → 7-Isopropyl-3-oxa-7,9-diaza-bicyclo[3.3.1]nonane

https://huagongshe.com/reaction/1778468

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsopropyl iodideHCID 6362—
EduktPotassium CarbonateHCID 11430—
Edukt3-Oxa-7,9-diaza-bicyclo[3.3.1]nonane-9-carboxylic acid benzyl esterHCID 67356121—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt7-Isopropyl-3-oxa-7,9-diaza-bicyclo[3.3.1]nonaneHCID 11769794657%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a solution of 3-oxa-7,9-diaza-bicyclo[3.3.1]nonane-9-carboxylic acid benzyl ester (Compound X) (100 mg, 0.33 mmol) in DMF (5 mL) was added K2CO3 (91 mg, 0.66 mmol) and 2-iodopropane (111 mg, 0.66 mmol). The reaction mixture was heated to 80° C. and stirred for 16 hours. The mixture was diluted with EtOAc (60 mL), and then washed with sat. NH4Cl, sat. NaHCO3 and brine (20 mL) respectively. The organic layer was dried over Na2SO4, and then concentrated to give the crude product which was dissolved in MeOH (20 mL). To the solution was added 10% Pd on carbon (20 mg). The mixture was stirred under one atmosphere pressure of H2 at room temperature. After the reaction was completed, the mixture was filtered and concentrated to give the crude 7-isopropyl-3-oxa-7,9-diaza-bicyclo[3.3.1]nonane (Compound AA) (32 mg, 57%) which was directly used for next step. MS: calc'd (MH+) 171, measured (MH+) 171.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09266904B2
Quelldatensatzuspto-grants-2016_02
ORD IDord-bb2d72ad376c4942aba01062546f105c
Quellennotizuspto-grants-2016_02