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Potassium Carbonate → (R)-2-(5-bromopyridin-3-ylamino)-3-methyl-N-(2,2,2-trifluoroethyl)butanamide

HRID 510179
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 510179
Cl.[NH2:2][C@H:3]([CH:12]([CH3:14])[CH3:13])[C:4]([NH:6][CH2:7][C:8]([F:11])([F:10])[F:9])=[O:5].[Br:15][C:16]1[CH:17]=[N:18][CH:19]=[C:20](Br)[CH:21]=1.C(=O)([O-])[O-].[K+].[K+]>CS(C)=O.C(OCC)(=O)C.[Cu]I>[Br:15][C:16]1[CH:21]=[C:20]([NH:2][C@H:3]([CH:12]([CH3:14])[CH3:13])[C:4]([NH:6][CH2:7][C:8]([F:9])([F:10])[F:11])=[O:5])[CH:19]=[N:18][CH:17]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 3

HCID 11430Potassium CarbonateHCID 693693,5-DibromopyridineHCID 117628603(R)-2-amino-3-methyl-N-(2,2,2-trifluoroethyl)butanamide hydrochloride

Produkt 1

HCID 89495326(R)-2-(5-bromopyridin-3-ylamino)-3-methyl-N-(2,2,2-trifluoroethyl)butanamideAusbeute 46,4 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 24350
Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)
Katalysator
HCID 679Dimethyl SulfoxideLösungsmittel
HCID 8857Ethyl AcetateLösungsmittel

Reaktionsbedingungen

Temperatur
120 °C

Versuchsvorschrift

In a round bottomed flask equipped with a magnetic stirrer, (R)-2-amino-3-methyl-N-(2,2,2-trifluoroethyl)butanamide hydrochloride (1-3b) (20 g, 85 mmol), 3,5-Dibromopyridine (30.3 g, 128 mmol), Potassium carbonate (35.3 g, 256 mmol) were suspended in DMSO (71 ml, 1.2M) and reaction mixture was purged with nitrogen for 20 minutes, then Copper(I) Iodide (0.974 g, 5.1 mmol) was added and the reaction mixture was slowly heated to 120° C. overnight. The cooled reaction mixture was then partitioned between Isopropanol (IPA):Chloroform (1:3) and Water, the aqueous layer was extracted with three times with IPA:Chloroform mixture. The combined organic layers were extracted with 1M solution of EDTA disodium salt, dried over anhydrous magnesium sulfate, filtered and concentrated to give the crude sample. Purification on a silica gel column using a gradient 0-40% ethyl acetate:hexane gave an orange solid which was taken up in ethyl acetate and concentrated to an oil, hexane was added dropwise while stirring, a white solid crystallized which was filtered, washed with hexane and dried under vacuum to give 14 g, (46.4%) the title compound, I-3, as a white solid.

Aufarbeitung

  1. customIn a round bottomed flask equipped with a magnetic stirrer
  2. customreaction mixture
  3. customwas purged with nitrogen for 20 minutes
  4. customThe cooled reaction mixture
  5. customwas then partitioned between Isopropanol (IPA)
  6. extractionChloroform (1:3) and Water, the aqueous layer was extracted with three times with IPA
  7. extractionThe combined organic layers were extracted with 1M solution of EDTA disodium salt
  8. dry with materialdried over anhydrous magnesium sulfate
  9. filtrationfiltered
  10. concentrationconcentrated
  11. customto give the crude sample
  12. customPurification on a silica gel column
  13. customhexane gave an orange solid which
  14. concentrationconcentrated to an oil, hexane
  15. additionwas added dropwise
  16. customa white solid crystallized which
  17. filtrationwas filtered
  18. washwashed with hexane
  19. customdried under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-52c25ea0d8064d0bae63f8de594bf526
Quelldatensatz
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09096598B2

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