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1-(2-Amino-1,3-thiazol-5-yl)cyclobutan-1-ol → 5-Cyclobutyl-1,3-thiazol-2-amine

HRID 2085489
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2085489
[NH2:1][C:2]1[S:3][C:4]([C:7]2(O)[CH2:10][CH2:9][CH2:8]2)=[CH:5][N:6]=1>FC(F)(F)C(O)=O.[OH-].[OH-].[Pd+2]>[CH:7]1([C:4]2[S:3][C:2]([NH2:1])=[N:6][CH:5]=2)[CH2:10][CH2:9][CH2:8]1
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Komponenten

4

Edukt 1

HCID 227313761-(2-Amino-1,3-thiazol-5-yl)cyclobutan-1-ol

Produkt 1

HCID 129914235-Cyclobutyl-1,3-thiazol-2-amineAusbeute 79 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 9942167Palladium hydroxideKatalysatorHCID 6422Trifluoroacetic acidLösungsmittel

Versuchsvorschrift

A solution of 1-(2-amino-thiazol-5-yl)cyclobutanol (Preparation 1; 6.6 g, 39 mmol) in trifluoroacetic acid (150 mL) was treated with 20% palladium hydroxide on carbon (2.3 g). The mixture was evacuated and purged with nitrogen (3 times), then was evacuated and purged with hydrogen gas (50 psi). The mixture was shaken for 24 hours and was evacuated and purged with nitrogen. The mixture was then filtered through Celite which was rinsed with methanol. The organic solvent was removed in vacuo, ethylacetate was added, followed by 29% ammonium hydroxide solution. The aqueous and organic layers were separated and the aqueous layer was extracted with ethylacetate. The combined organic layers were washed with brine, were dried (MgSO4), were filtered, and the solvent was removed in vacuo. The resulting residue was purified by silica gel chromatography (40:1:1 CHCl3—MeOH—NH4OH) to afford 4.75 g of 5-cyclobutyl-thiazol-2-ylamine, the title compound. 1HNMR (400 MHz, DMSO-d6): 6.66(s,2H), 6.57(s, 2H), 3.43 (m,1H), 2.20 (m,2H), 1.98-1.7 (m,4H).

Aufarbeitung

  1. customThe mixture was evacuated
  2. custompurged with nitrogen (3 times)
  3. customwas evacuated
  4. custompurged with hydrogen gas (50 psi)
  5. customwas evacuated
  6. custompurged with nitrogen
  7. filtrationThe mixture was then filtered through Celite which
  8. washwas rinsed with methanol
  9. customThe organic solvent was removed in vacuo, ethylacetate
  10. additionwas added
  11. customThe aqueous and organic layers were separated
  12. extractionthe aqueous layer was extracted with ethylacetate
  13. washThe combined organic layers were washed with brine
  14. dry with materialwere dried (MgSO4)
  15. filtrationwere filtered
  16. customthe solvent was removed in vacuo
  17. customThe resulting residue was purified by silica gel chromatography (40:1:1 CHCl3—MeOH—NH4OH)

Quellen und Nachweise

ORD-Eintrag
ord-1943e7c6151e4f8cb49a5227acd7e5d0
Quelldatensatz
uspto-grants-2004_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06720427B2

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