Water → 2-(Quinoxalin-6-yl)-1-(4-(3-(trifluoromethyl)-phenyl)piperidino)ethanone

HRID 2052982Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2052982
[N:1]1[C:10]2[C:5](=[CH:6][C:7]([CH2:11][C:12]([OH:14])=O)=[CH:8][CH:9]=2)[N:4]=[CH:3][CH:2]=1.Cl.[F:16][C:17]([F:31])([F:30])[C:18]1[CH:19]=[C:20]([CH:24]2[CH2:29][CH2:28][NH:27][CH2:26][CH2:25]2)[CH:21]=[CH:22][CH:23]=1.O>CN(C=O)C.F[P-](F)(F)(F)(F)F.N1(O[P+](N(C)C)(N(C)C)N(C)C)C2C=CC=CC=2N=N1>[N:1]1[C:10]2[C:5](=[CH:6][C:7]([CH2:11][C:12]([N:27]3[CH2:28][CH2:29][CH:24]([C:20]4[CH:21]=[CH:22][CH:23]=[C:18]([C:17]([F:16])([F:30])[F:31])[CH:19]=4)[CH2:25][CH2:26]3)=[O:14])=[CH:8][CH:9]=2)[N:4]=[CH:3][CH:2]=1

Komponenten

6

Versuchsvorschrift

0.48 g (2.55 mmol) of quinoxalin-6-ylacetic acid is mixed in 25 ml of DMF, and 1.07 ml of TEA, 0.68 g (2.55 mmol) of 4-(3-(trifluoromethyl)phenyl)piperidine hydrochloride and 1.13 mg of BOP are added thereto. The mixture is heated at ambient temperature overnight, 200 ml of water are added and extraction is carried out with ethyl acetate. The organic phase is dried over sodium sulfate and filtered, and the solvent is evaporated under reduced pressure. A dark oil is thus obtained, which oil is purified by flash chromatography on a column of silica gel, elution being carried out with ethyl acetate. 0.76 g of the title product is obtained in the form of a yellow oil.

Aufarbeitung

  1. extractionextraction
  2. dry with materialThe organic phase is dried over sodium sulfate
  3. filtrationfiltered
  4. customthe solvent is evaporated under reduced pressure
  5. customA dark oil is thus obtained
  6. customwhich oil is purified by flash chromatography on a column of silica gel, elution

Quellen und Nachweise

ORD-Eintrag
ord-d2042c9196374f709806d9079233e2b5
Quelldatensatz
uspto-grants-2008_02
Patentnummer
US07326720B2

Notizen zur Reaktion

Wird geladen…