Sodium Carbonate → HCID 11462486, Verbindung

HRID 1247449Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1247449
CC1(C)C(C)(C)OB([C:9]2[CH:17]=[CH:16][CH:15]=[C:14]3[C:10]=2[CH2:11][NH:12][C:13]3=[O:18])O1.Br[C:21]1[N:26]=[CH:25][C:24]([NH:27][C:28]([NH:30][C:31]2[CH:36]=[CH:35][CH:34]=[C:33]([CH3:37])[CH:32]=2)=[O:29])=[CH:23][CH:22]=1.NC1C=C(Br)C=CN=1.C1(C)C=CC=C(N=C=O)C=1.C([O-])([O-])=O.[Na+].[Na+]>C1(C)C=CC=CC=1.O.C(OCC)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>[CH3:37][C:33]1[CH:32]=[C:31]([NH:30][C:28]([NH:27][C:24]2[CH:25]=[N:26][C:21]([C:9]3[CH:17]=[CH:16][CH:15]=[C:14]4[C:10]=3[CH2:11][NH:12][C:13]4=[O:18])=[CH:22][CH:23]=2)=[O:29])[CH:36]=[CH:35][CH:34]=1

Komponenten

10

Edukt 5

HCID 10340Sodium CarbonateHCID 69303m-Tolyl isocyanateHCID 6932822-Amino-4-bromopyridineHCID 219075244-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydro-1H-isoindol-1-oneHCID 21907539HCID 21907539, Verbindung

Produkt 1

HCID 11462486HCID 11462486, VerbindungAusbeute 14,2 %

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 178418397HCID 178418397, VerbindungKatalysatorHCID 962WaterLösungsmittelHCID 1140TolueneLösungsmittelHCID 3283Diethyl EtherLösungsmittel

Versuchsvorschrift

A solution of Example 54A (259 mg, 1 mmol) and N-(6-bromo-3-pyridinyl)-N′-(3-methylphenyl)urea (367 mg, 1.2 mmol) (prepared from 2-amino-4-bromopyridine and m-tolylisocyanate following the procedure of Example 1E) in toluene (6 mL) and ethanol (6 mL) was degassed with N2 then treated sequentially with a solution of Na2CO3 (509 mg, 4.8 mmol) in water (3 mL) and tetrakis(triphenylphosphine)palladium (0) (208 mg, 0.187 mmol) and stirred at reflux overnight. The resulting suspension was cooled to room temperature, diluted with diethyl ether, and filtered. The filter cake was washed with water, diethyl ether, dichloromethane, ethyl acetate, and methanol. The combined filtrates were concentrated to give 51 mg of the desired product. 1H NMR (300 MHz, DMSO-d6) δ 10.35 (s,1H), 9.58 (s,1H), 8.73 (s, 1H), 8.56 (s,1H), 8.06 (d, J=6 Hz, 1H), 7.56–7.81 (m, 4H), 7.3–7.46 (m, 2H), 7.20 (t, J=6 Hz, 1H), 6.85 (d, J=6 Hz, 1H), 4.56 (s, 2H), 2.31 (s,3H); MS (ESI(+)) m/e 359 (M+H)+.

Aufarbeitung

  1. customethanol (6 mL) was degassed with N2
  2. temperatureat reflux overnight
  3. filtrationfiltered
  4. washThe filter cake was washed with water, diethyl ether, dichloromethane, ethyl acetate, and methanol
  5. concentrationThe combined filtrates were concentrated

Quellen und Nachweise

ORD-Eintrag
ord-3974da0a13f040d4b4cb6919e4a07e55
Quelldatensatz
uspto-grants-2006_10
Patentnummer
US07129260B2

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