Dimethylformamide → Methyl 3-cyano-1H-indazole-5-carboxylate

HRID 1892597Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1892597
Br[C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][N:6]=[C:5]2[C:11]#[N:12].[C:13]([O-:16])(=[O:15])C.[Na+].[CH3:18]N(C)C=O>CO>[C:11]([C:5]1[C:4]2[C:8](=[CH:9][CH:10]=[C:2]([C:13]([O:16][CH3:18])=[O:15])[CH:3]=2)[NH:7][N:6]=1)#[N:12]

Komponenten

5

Edukt 3

HCID 6228DimethylformamideHCID 517045Sodium AcetateHCID 247289115-bromo-1H-indazole-3-carbonitrile

Produkt 1

HCID 44632177Methyl 3-cyano-1H-indazole-5-carboxylateAusbeute 68 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

A suspension of 5-bromo-3-cyanoindazole (3 g, 13.51 mmol) palladium dichloride 1,1′-bis(diphenylphosphino)ferrocene (1.76 g, 2.16 mmol), sodium acetate (3.32 g, 40.5 mmol), dimethylformamide (1 mL) in methanol (100 mL) was degassed, and kept under carbon monoxide (80 psi) pressure at 80° C. in a autoclave for 16 hours. The mixture was diluted with water (50 mL), filtered through Celite® bed and the filtrate was concentrated. The obtained residue was acidified with 10% citric acid solution and extracted with ethyl acetate (2×100 mL). The combined organic layers were washed with brine (50 mL), dried over anhydrous sodium sulfate and concentrated. The obtained crude product was purified by column chromatography (100-200 mesh silica gel) using 10% ethyl acetate in chloroform as eluent to afford methyl 3-cyano-1H-indazole-5-carboxylate (1.8 g, 68%) as a solid. 1HNMR (CDCl3) δ ppm 10.8 (s, 1H), 8.7 (s, 1H), 8.22 (d, 1H), 7.64 (d, 1H), 4.0 (s, 3H).

Aufarbeitung

  1. customwas degassed
  2. customat 80° C.
  3. customfor 16 hours
  4. additionThe mixture was diluted with water (50 mL)
  5. filtrationfiltered through Celite® bed
  6. concentrationthe filtrate was concentrated
  7. extractionextracted with ethyl acetate (2×100 mL)
  8. washThe combined organic layers were washed with brine (50 mL)
  9. dry with materialdried over anhydrous sodium sulfate
  10. concentrationconcentrated
  11. customThe obtained crude product
  12. customwas purified by column chromatography (100-200 mesh silica gel)

Quellen und Nachweise

ORD-Eintrag
ord-e1e5ea9d010f479f90748ef0c4181ee1
Quelldatensatz
uspto-grants-2013_08
Patentnummer
US08507681B2

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