Sodium Bicarbonate → 3-Oxa-8-azabicyclo[3.2.1]oct-8-yl(8-(1,3-oxazol-5-yl)-6-(trifluoromethyl)imidazo[1,2-a]pyridin-3-yl)methanone

HRID 931049Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 931049
[O:1]1[C:5]([C:6]2[C:7]3[N:8]([C:16]([C:19]([OH:21])=O)=[CH:17][N:18]=3)[CH:9]=[C:10]([C:12]([F:15])([F:14])[F:13])[CH:11]=2)=[CH:4][N:3]=[CH:2]1.F[P-](F)(F)(F)(F)F.C(C(=NO[C+](N(C)C)N1CCOCC1)C(OCC)=O)#N.Cl.[CH:50]12[NH:57][CH:54]([CH2:55][CH2:56]1)[CH2:53][O:52][CH2:51]2.C(=O)(O)[O-].[Na+]>CN(C=O)C.C(N(CC)CC)C>[CH:54]12[N:57]([C:19]([C:16]3[N:8]4[CH:9]=[C:10]([C:12]([F:13])([F:14])[F:15])[CH:11]=[C:6]([C:5]5[O:1][CH:2]=[N:3][CH:4]=5)[C:7]4=[N:18][CH:17]=3)=[O:21])[CH:50]([CH2:56][CH2:55]1)[CH2:51][O:52][CH2:53]2

Komponenten

7

Versuchsvorschrift

To a mixture of 8-(1,3-oxazol-5-yl)-6-(trifluoromethyl)imidazo[1,2-a]pyridine-3-carboxylic acid (80 g), triethylamine (113 mL) and DMF (2000 mL) were added (1-cyano-2-ethoxy-2-oxoethylideneaminooxy)dimethylamino-morpholino-carbenium hexafluorophosphate (127 g) and 3-oxa-8-azabicyclo[3.2.1]octane hydrochloride (42.3 g) at 0° C., and the mixture was stirred at room temperature for 1 hr. To the reaction mixture was added saturated aqueous sodium bicarbonate solution at 0° C. The obtained solid was collected by filtration, and washed with saturated aqueous sodium bicarbonate solution, water, ethanol and methyl tert-butyl ether to give the title compound (104 g).

Aufarbeitung

  1. filtrationThe obtained solid was collected by filtration
  2. washwashed with saturated aqueous sodium bicarbonate solution, water, ethanol and methyl tert-butyl ether

Quellen und Nachweise

ORD-Eintrag
ord-13d0acf4265a4864b296c714245693bb
Quelldatensatz
uspto-grants-2016_03
Patentnummer
US09296746B2

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