Sodium Carbonate → HCID 178422653, Verbindung

HRID 1517098Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1517098
COC1C=CC(C[N:8]2[CH:12]=[C:11]([C:13]3[N:18]=[C:17]([C:19]([N:21]4[CH2:26][CH2:25][CH:24]([N:27]5[CH2:31][CH2:30][CH2:29][CH2:28]5)[CH2:23][CH2:22]4)=[O:20])[C:16]([CH3:32])=[CH:15][C:14]=3[C:33]3[CH:38]=[CH:37][CH:36]=[C:35]([C:39]([F:42])([F:41])[F:40])[CH:34]=3)[N:10]=[N:9]2)=CC=1.C([O-])([O-])=O.[Na+].[Na+]>FC(F)(F)C(O)=O>[CH3:32][C:16]1[C:17]([C:19]([N:21]2[CH2:22][CH2:23][CH:24]([N:27]3[CH2:31][CH2:30][CH2:29][CH2:28]3)[CH2:25][CH2:26]2)=[O:20])=[N:18][C:13]([C:11]2[N:10]=[N:9][NH:8][CH:12]=2)=[C:14]([C:33]2[CH:38]=[CH:37][CH:36]=[C:35]([C:39]([F:42])([F:41])[F:40])[CH:34]=2)[CH:15]=1

Komponenten

4

Versuchsvorschrift

0.30 g (0.50 mmol) of [6-[1-(4-methoxy-benzyl)-1H-[1,2,3]triazol-4-yl]-3-methyl-5-(3-trifluoromethyl-phenyl)-pyridin-2-yl]-(4-pyrrolidin-1-yl-piperidin-1-yl)-methanone (intermediate 13) in 3.2 ml of trifluoroacetic acid were stirred at reflux for 23 hours. The reaction mixture was then poured into crashed ice, the pH was adjusted to 8-9 with aqueous Na2CO3 and the mixture was extracted twice with CH2Cl2; the organic phases were washed with water, dried over magnesium sulfate, filtered and evaporated. The residue was purified by flash column chromatography (CH2Cl2/MeOH 98:2 to 4:1) to give 0.19 g (77%) of the title compound as an off-white solid. MS: 485.4 (MH+).

Aufarbeitung

  1. temperatureat reflux for 23 hours
  2. additionThe reaction mixture was then poured
  3. extractionthe mixture was extracted twice with CH2Cl2
  4. washthe organic phases were washed with water
  5. dry with materialdried over magnesium sulfate
  6. filtrationfiltered
  7. customevaporated
  8. customThe residue was purified by flash column chromatography (CH2Cl2/MeOH 98:2 to 4:1)

Quellen und Nachweise

ORD-Eintrag
ord-7108f1db531040c5b01e68b787ae87f8
Quelldatensatz
uspto-grants-2012_07
Patentnummer
US08227613B2

Notizen zur Reaktion

Wird geladen…