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Morpholine → (1-Benzyl-3-bromo-4-methyl-5-(trifluoromethyl)-1H-pyrrol-2-yl)(morpholino)methanone

HRID 623789
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 623789
CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C.[CH2:34]([N:41]1[C:45]([C:46]([F:49])([F:48])[F:47])=[C:44]([CH3:50])[C:43]([Br:51])=[C:42]1[C:52]([OH:54])=O)[C:35]1[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=1.[NH:55]1[CH2:60][CH2:59][O:58][CH2:57][CH2:56]1>CN(C=O)C.CCOC(C)=O.O>[CH2:34]([N:41]1[C:45]([C:46]([F:47])([F:48])[F:49])=[C:44]([CH3:50])[C:43]([Br:51])=[C:42]1[C:52]([N:55]1[CH2:60][CH2:59][O:58][CH2:57][CH2:56]1)=[O:54])[C:35]1[CH:36]=[CH:37][CH:38]=[CH:39][CH:40]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 4

HCID 8083MorpholineHCID 81531DiisopropylethylamineHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 867118651-Benzyl-3-bromo-4-methyl-5-(trifluoromethyl)-1H-pyrrole-2-carboxylic acid

Produkt 1

HCID 86711874
(1-Benzyl-3-bromo-4-methyl-5-(trifluoromethyl)-1H-pyrrol-2-yl)(morpholino)methanone
Ausbeute 84 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 962WaterLösungsmittelHCID 6228DimethylformamideLösungsmittelHCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

HATU (12.59 g 33.14 mmol) and DIPEA (12.3 mL, 33.14 mmol) were added to the ice cold solution of 1-benzyl-3-bromo-4-methyl-5-(trifluoromethyl)-1H-pyrrole-2-carboxylic acid (10 g, 27.62 mmol) in DMF (110 mL) and it was stirred for 10 min at same temperature and then morpholine (2.8 mL, 33.14 mmol) was added to the reaction mixture warmed to RT and then stirred for 14 h. The reaction mixture was diluted with EtOAc and H2O. The aqueous layer was extracted with EtOAc (2×300 mL), washed with water (2×300 mL) and brine (2×300 mL), organic layer was dried over anhydrous Na2SO4, combined organic layer was dried over anhydrous Na2SO4 and concentrated under reduced pressure to yield crude mass which was then purified by column chromatography (100-200 mesh Silica gel; 30% ethyl acetate/hexane; Rf-value 0.6) to afford title compound (10 g, 84% yield, white color solid).

Aufarbeitung

  1. stirringstirred for 14 h
  2. extractionThe aqueous layer was extracted with EtOAc (2×300 mL)
  3. washwashed with water (2×300 mL) and brine (2×300 mL), organic layer
  4. dry with materialwas dried over anhydrous Na2SO4
  5. dry with materialwas dried over anhydrous Na2SO4
  6. concentrationconcentrated under reduced pressure
  7. customto yield crude mass which
  8. customwas then purified by column chromatography (100-200 mesh Silica gel; 30% ethyl acetate/hexane; Rf-value 0.6)

Quellen und Nachweise

ORD-Eintrag
ord-76a414e6f0474300864a3ee493e0cf6e
Quelldatensatz
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09302988B2

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