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Cesium fluoride → 4-Acetylamino-3-chloro-6-(2,4-difluoro-3-methylphenyl)-pyridine-2-carboxylic acid methyl ester

HRID 2249389
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2249389
Br[C:2]1[CH:7]=[CH:6][C:5]([F:8])=[C:4]([CH3:9])[C:3]=1[F:10].[CH3:11][O:12][C:13]([C:15]1[C:20]([Cl:21])=[C:19]([NH:22][C:23](=[O:25])[CH3:24])[CH:18]=[C:17]([Sn](C)(C)C)[N:16]=1)=[O:14].C1(P(C2C=CC=CC=2)CCCCP(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[F-].[Cs+]>C(#N)C.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[CH3:11][O:12][C:13]([C:15]1[C:20]([Cl:21])=[C:19]([NH:22][C:23](=[O:25])[CH3:24])[CH:18]=[C:17]([C:2]2[CH:7]=[CH:6][C:5]([F:8])=[C:4]([CH3:9])[C:3]=2[F:10])[N:16]=1)=[O:14]
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Komponenten

7

Edukt 4

HCID 25953Cesium fluorideHCID 821241,4-Bis(diphenylphosphino)butaneHCID 112872263-Bromo-2,6-difluorotolueneHCID 226773084-Acetylamino-3-chloro-6-trimethylstannylpyridine-2-carboxylic acid methyl ester

Produkt 1

HCID 685975834-Acetylamino-3-chloro-6-(2,4-difluoro-3-methylphenyl)-pyridine-2-carboxylic acid methyl ester
Ausbeute 20 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 167845palladium(II) acetateKatalysatorHCID 6342AcetonitrileLösungsmittel

Versuchsvorschrift

A solution of 1-bromo-2,4-difluoro-3-methylbenzene (2.10 g, 0.09 mol), 4-acetylamino-3-chloro-6-trimethylstannylpyridine-2-carboxylic acid methyl ester (4.00 g, 0.01 mol), 1,4-bis(diphenylphosphino)butane (0.140 g, 0.0003 mol) and cesium fluoride (4.5 g, 0.03 mol) in acetonitrile (100 mL) was degassed with nitrogen. Palladium acetate (0.70 g, 0.0003 mol) was added the solution heated to reflux for 2 hours. The reaction mixture was filtered through celite and the filtrate diluted with water (200 mL) and then extracted with ethyl acetate (2×150 mL). The combined organic phases were dried and concentrated and the residual solid was purified by chromatography (50% ethyl acetate in hexanes) to give 4-acetylamino-3-chloro-6-(2,4-difluoro-3-methylphenyl)-pyridine-2-carboxylic acid methyl ester (0.800 g, 0.002 mol): mp 152-153° C.

Aufarbeitung

  1. temperatureheated
  2. temperatureto reflux for 2 hours
  3. filtrationThe reaction mixture was filtered through celite
  4. additionthe filtrate diluted with water (200 mL)
  5. extractionextracted with ethyl acetate (2×150 mL)
  6. customThe combined organic phases were dried
  7. concentrationconcentrated
  8. customthe residual solid was purified by chromatography (50% ethyl acetate in hexanes)

Quellen und Nachweise

ORD-Eintrag
ord-21d1a8902407494c859cb3b17d111e9a
Quelldatensatz
uspto-grants-2008_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07314849B2

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