HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 522228Erstellt: 24. Oktober 2026
Sodium Bicarbonate → 1,1-dimethylethyl 4-[4-bromo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-2-yl]-3,6-dihydro-1(2H)-pyridinecarboxylate
https://huagongshe.com/de/reaction/522228
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | Tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine-1-carboxylate | HCID 4642098 | — |
| Edukt | 4-Bromo-2-iodo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine | HCID 46907955 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 1,1-dimethylethyl 4-[4-bromo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-2-yl]-3,6-dihydro-1(2H)-pyridinecarboxylate | HCID 69001059 | — |
Reaktionsschritte
A mixture of Example 135B (260.0 mg, 0.561 mmol), tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate (191 mg, 0.618 mmol), Pd(Ph3P)4 (32.4 mg, 0.028 mmol), and saturated sodium bicarbonate solution (2 mL, 0.561 mmol) in N,N-dimethylformamide (8 mL) was purged with nitrogen and heated at 80° C. for 4 hours. The mixture was partitioned between ethyl acetate and brine. The organic layer was washed with brine, dried over MgSO4, and filtered. The filtrate was concentrated and the residue was separated by flash chromatography on silica gel (Teledyne CombiFlash Rf, 40% to 100% ethyl acetate in hexane) to provide the title compound. MS (ESI+) m/z 306 (M+1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09328112B2 |
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| Quelldatensatz | uspto-grants-2016_05 |
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| ORD ID | ord-9fc930466c024cfe8fe618bb8010fcb3 |
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| Quellennotiz | uspto-grants-2016_05 |
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