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HRID 75312Erstellt: 24. Oktober 2026

Binap, (A+-)- → 1-Methyl-6-(2-oxa-6-azaspiro[3,3]heptan-6-yl)-1H-pyrrolo[3,2-b]pyridine-5-carbonitrile

https://huagongshe.com/de/reaction/75312

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBinap, (A+-)-HCID 634876—
EduktSodium t-butoxideHCID 23676156—
Edukt6-Bromo-1-methyl-1H-pyrrolo[3,2-b]pyridine-5-carbonitrileHCID 86707963—
Edukt2-Azaspiro[3.3]heptan-6-oneHCID 86708012—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelDimethylacetamideHCID 31374—
Produkt1-Methyl-6-(2-oxa-6-azaspiro[3,3]heptan-6-yl)-1H-pyrrolo[3,2-b]pyridine-5-carbonitrileHCID 8670801169%

Reaktionsbedingungen

Temperatur102 °C

Reaktionsschritte

6-Bromo-1-methyl-1H-pyrrolo[3,2-b]pyridine 5-carbonitrile (300 mg, 1.27 mmol), sodium tert-butoxide (366 mg, 3.81 mmol), racemic BINAP (79 mg, 0.127 mmol), Pd2 dba3 (58 mg, 0.064 mmol), and 2-oxo-6-azaspiro[3,3]heptane, 0.5 oxylic acid salt (274 mg, 1.91 mmol) were combined in DMA (12 mL) under N2. The reaction mixture was heated at 102° C. in a microwave for 1 hour and was then diluted with DCM, washed with brine, dried over MgSO4, and concentrated. Purification by silica gel chromatography (2-5% MeOH in DCM) gave the title compound as a pale yellow solid (222 mg, 69%). 1H NMR (500 MHz, CDCl3) δ ppm 7.21 (d, 1H, J=3.5 Hz), 6.60 (s, 1H), 6.58 (d, 1H, J=3.5 Hz), 4.89 (s, 4H), 4.34 (s, 4H), 3.73 (s, 3H). ESI-MS m/z [M+H]+ calc'd for C14H14F4O, 255; found 255.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08835420B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-bdbf1c354c124e98a8cb90f3e907f08f
Quellennotizuspto-grants-2014_09