Acryloyl chloride → N-(5-Bromo-2-(2,5-dimethyl-1H-pyrrol-1-yl)-6-methylpyrimidin-4-yl)-N-(pyrrolidin-1-yl)acrylamide

HRID 641684Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 641684
[Br:1][C:2]1[C:3]([NH:16][N:17]2[CH2:21][CH2:20][CH2:19][CH2:18]2)=[N:4][C:5]([N:9]2[C:13]([CH3:14])=[CH:12][CH:11]=[C:10]2[CH3:15])=[N:6][C:7]=1[CH3:8].[C:22](Cl)(=[O:25])[CH:23]=[CH2:24]>C(Cl)Cl.CCN(C(C)C)C(C)C>[Br:1][C:2]1[C:3]([N:16]([N:17]2[CH2:21][CH2:20][CH2:19][CH2:18]2)[C:22](=[O:25])[CH:23]=[CH2:24])=[N:4][C:5]([N:9]2[C:13]([CH3:14])=[CH:12][CH:11]=[C:10]2[CH3:15])=[N:6][C:7]=1[CH3:8]

Komponenten

5

Edukt 2

HCID 13140Acryloyl chlorideHCID 592589815-Bromo-2-(2,5-dimethyl-1H-pyrrol-1-yl)-6-methyl-N-(pyrrolidin-1-yl)pyrimidin-4-amine

Produkt 1

HCID 59258866N-(5-Bromo-2-(2,5-dimethyl-1H-pyrrol-1-yl)-6-methylpyrimidin-4-yl)-N-(pyrrolidin-1-yl)acrylamide

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6344DichloromethaneLösungsmittel2×HCID 81531DiisopropylethylamineLösungsmittel

Versuchsvorschrift

To a reaction solution of 5-bromo-2-(2,5-dimethyl-1H-pyrrol-1-yl)-6-methyl-N-(pyrrolidin-1-yl)pyrimidin-4-amine (3.14 g, 8.97 mmol) in anhydrous methylene chloride (120 ml) and hunig's base (4.68 ml) was added slowly a solution of acryloyl chloride (0.80 ml, 9.86 mmol) in methylene chloride (30 ml) dropwise at R.T. After stirring at R.T for 60 mins, the reaction mixture was concentrated under reduced pressure and the residue was purified by 120 g column eluted with 40% ethyl acetate:hexane to give the titled product weighted 3.5 g a white solid 97%

Aufarbeitung

  1. concentrationthe reaction mixture was concentrated under reduced pressure
  2. customthe residue was purified by 120 g column
  3. washeluted with 40% ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-6f730ab8596745b09eccab0cb89283c4
Quelldatensatz
uspto-grants-2010_04
Patentnummer
US07696213B2

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