HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Binap, (A+-)- | HCID 634876 | — |
| Edukt | Sodium t-butoxide | HCID 23676156 | — |
| Edukt | 6-Bromo-1-methyl-1H-pyrrolo[3,2-b]pyridine-5-carbonitrile | HCID 86707963 | — |
| Edukt | 2-Azaspiro[3.3]heptan-6-one | HCID 86708012 | — |
| Katalysator | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Dimethylacetamide | HCID 31374 | — |
| Produkt | 1-Methyl-6-(2-oxa-6-azaspiro[3,3]heptan-6-yl)-1H-pyrrolo[3,2-b]pyridine-5-carbonitrile | HCID 86708011 | 69% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08835420B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-bdbf1c354c124e98a8cb90f3e907f08f |
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| Quellennotiz | uspto-grants-2014_09 |
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