(3,5-bis-trifluoromethyl-benzyl)-[6-(cyclopentylmethyl-ethyl-amino)-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine-5-ylmethyl]-carbamic acid methyl ester → [(3,5-Bis-trifluoromethyl-benzyl)-(2-pentyl-quinolin-3-ylmethyl)-amino]-acetic acid tert-butyl ester

HRID 1911751Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1911751
COC(=O)N(CC1C=C(C(F)(F)F)C=C(C(F)(F)F)C=1)CC1C=C2C(C)=NN(C)C2=NC=1N(CC1CCCC1)CC.[C:42]([O:46][C:47](=[O:81])[CH2:48][N:49]([CH2:66][C:67]1[CH:72]=[C:71]([C:73]([F:76])([F:75])[F:74])[CH:70]=[C:69]([C:77]([F:80])([F:79])[F:78])[CH:68]=1)[CH2:50][C:51]1[C:52]([C:61]#[C:62][CH2:63][CH2:64][CH3:65])=[N:53][C:54]2[C:59]([CH:60]=1)=[CH:58][CH:57]=[CH:56][CH:55]=2)([CH3:45])([CH3:44])[CH3:43]>C(O)C.[Pd]>[C:42]([O:46][C:47](=[O:81])[CH2:48][N:49]([CH2:66][C:67]1[CH:72]=[C:71]([C:73]([F:76])([F:75])[F:74])[CH:70]=[C:69]([C:77]([F:78])([F:79])[F:80])[CH:68]=1)[CH2:50][C:51]1[C:52]([CH2:61][CH2:62][CH2:63][CH2:64][CH3:65])=[N:53][C:54]2[C:59]([CH:60]=1)=[CH:58][CH:57]=[CH:56][CH:55]=2)([CH3:43])([CH3:44])[CH3:45]

Komponenten

5

Edukt 2

HCID 11671498(3,5-bis-trifluoromethyl-benzyl)-[6-(cyclopentylmethyl-ethyl-amino)-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine-5-ylmethyl]-carbamic acid methyl esterHCID 57486794[(3,5-Bis-trifluoromethyl-benzyl)-(2-pent-1-ynyl-quinolin-3-ylmethyl)-amino]-acetic acid tert-butyl ester

Produkt 1

HCID 57473632[(3,5-Bis-trifluoromethyl-benzyl)-(2-pentyl-quinolin-3-ylmethyl)-amino]-acetic acid tert-butyl esterAusbeute 45 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23938PalladiumKatalysatorHCID 702EthanolLösungsmittel2×

Versuchsvorschrift

The compound obtained in Example 16, [(3,5-bis-trifluoromethyl-benzyl)-(2-pent-1-ynyl-quinolin-3-ylmethyl)-amino]-acetic acid tert-butyl ester (163 mg, 0.3 mmol) was dissolved in ethanol (3 mL), and palladium [10% on carbon powder (50 mg)] was added. The resulting mixture was stirred under H2 (using a balloon) for 3 h. The sample was diluted in ethanol and filtered through Celite™. The Celite™ was washed with ethanol, the filtrate was concentrated by rotary evaporation, and the resulting sample was dried overnight under vacuum and the crude was purified (Biotage Horizon HPFC chromatography system, SiO2, 80:20 hexanes: ethyl acetate) to give the titled product as a colorless oil (0.075 g, yield: 45%).

Aufarbeitung

  1. customfor 3 h
  2. filtrationfiltered through Celite™
  3. washThe Celite™ was washed with ethanol
  4. concentrationthe filtrate was concentrated by rotary evaporation
  5. customthe resulting sample was dried overnight under vacuum
  6. customthe crude was purified (Biotage Horizon HPFC chromatography system, SiO2, 80:20 hexanes: ethyl acetate)

Quellen und Nachweise

ORD-Eintrag
ord-240ef619b42f4d1dabf1be324e74a147
Quelldatensatz
uspto-grants-2013_12
Patentnummer
US08604055B2

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