Sodium Carbonate → 4-chloro-3-(3,5-dichloro-pyridin-2-yl)-N-(2-methoxy-phenyl)-benzamide

HRID 448888Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 448888
C([O-])([O-])=O.[Na+].[Na+].[Cl:7][C:8]1[CH:24]=[CH:23][C:11]([C:12]([NH:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2[O:21][CH3:22])=[O:13])=[CH:10][C:9]=1B1OC(C)(C)C(C)(C)O1.Br[C:35]1[C:40]([Cl:41])=[CH:39][C:38]([Cl:42])=[CH:37][N:36]=1>C1(C)C=CC=CC=1.CCO.C(OCC)(=O)C.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[Cl:7][C:8]1[CH:24]=[CH:23][C:11]([C:12]([NH:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2[O:21][CH3:22])=[O:13])=[CH:10][C:9]=1[C:35]1[C:40]([Cl:41])=[CH:39][C:38]([Cl:42])=[CH:37][N:36]=1

Komponenten

8

Edukt 3

HCID 10340Sodium CarbonateHCID 8170902-Bromo-3,5-dichloropyridineHCID 686032344-chloro-N-(2-methoxy-phenyl)-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzamide

Produkt 1

HCID 686027194-chloro-3-(3,5-dichloro-pyridin-2-yl)-N-(2-methoxy-phenyl)-benzamideAusbeute 67,1 %

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 178418397HCID 178418397, VerbindungKatalysatorHCID 702EthanolLösungsmittelHCID 1140TolueneLösungsmittelHCID 8857Ethyl AcetateLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

A solution of 2N Na2CO3 (5.85 mL) and Pd(PPh3)4 (340 mg, 0.29 mmol) was added to a degassed mixture of 4-chloro-N-(2-methoxy-phenyl)-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzamide (2.2 g, 5.85 mmol) and 2-bromo-3,5-dichloro-pyridine (1.47 g, 6.44 mmol) in toluene (30 mL) and EtOH (6 mL). The mixture was heated at 100° C. for 12 hrs. Upon cooling to room temperature, the mixture was diluted with ethyl acetate and washed with water and brine, and was dried over Na2SO4. After filtration and concentration the mixture was taken up in EtOAc, filtered, washed with EtOAc (3×), MeOH and ether to yield 1.6 g of 4-chloro-3-(3,5-dichloro-pyridin-2-yl)-N-(2-methoxy-phenyl)-benzamide. MS [M+H]+: 406.9; tR=3.03 min. (method 1)

Aufarbeitung

  1. temperatureUpon cooling to room temperature
  2. washwashed with water and brine
  3. dry with materialwas dried over Na2SO4
  4. filtrationAfter filtration and concentration the mixture
  5. filtrationfiltered
  6. washwashed with EtOAc (3×), MeOH and ether

Quellen und Nachweise

ORD-Eintrag
ord-99f8932a08854e4f84107bf35862cdb7
Quelldatensatz
uspto-grants-2013_07
Patentnummer
US08481738B2

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