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Trifluoroacetic acid → HCID 18348838, Verbindung

HRID 2268645
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2268645
C(Cl)(=O)C(Cl)=O.C(OC([N:14]([C:28]1[CH:33]=[CH:32][N:31]=[CH:30][CH:29]=1)[CH2:15][CH2:16][O:17][C:18]1[CH:19]=[C:20]([CH:24]=[C:25]([Cl:27])[CH:26]=1)[C:21]([OH:23])=O)=O)(C)(C)C.[CH2:34]([NH:36][C:37]1[CH:42]=[CH:41][CH:40]=[CH:39][C:38]=1[F:43])[CH3:35].CCN(C(C)C)C(C)C.[F:53][C:54]([F:59])([F:58])[C:55]([OH:57])=[O:56]>ClCCl.CN(C=O)C>[F:53][C:54]([F:59])([F:58])[C:55]([OH:57])=[O:56].[Cl:27][C:25]1[CH:24]=[C:20]([CH:19]=[C:18]([O:17][CH2:16][CH2:15][NH:14][C:28]2[CH:29]=[CH:30][N:31]=[CH:32][CH:33]=2)[CH:26]=1)[C:21]([N:36]([CH2:34][CH3:35])[C:37]1[CH:42]=[CH:41][CH:40]=[CH:39][C:38]=1[F:43])=[O:23]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 5

HCID 6422Trifluoroacetic acidHCID 65578Oxalyl chlorideHCID 81531DiisopropylethylamineHCID 2737180N-ethyl-2-fluoroanilineHCID 18348849Benzoic acid,3-chloro-5-[2-[[(1,1-dimethylethoxy)carbonyl]-4-pyridinylamino]ethoxy]-

Produkt 1

HCID 18348838
HCID 18348838, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6228DimethylformamideLösungsmittelHCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

2M Oxalyl chloride solution in dichloromethane (0.080 ml) and DMF (0.001 ml) were added to a suspension of 3-[2-(tert-butoxycarbonyl-pyridin-4-yl-amino)-ethoxy]-5-chloro-benzoic acid (0.050 g) in anhydrous dichloromethane (1 ml). The reaction was stirred at room temperature for 2 h then a solution of N-ethyl-2-fluoroaniline (0.029 g) DMAP (0.001 g) and DIPEA (0.070 ml) were added. The reaction mixture was stirred at room temperature for 16 h and then triflouroacetic acid (1 ml) was added. The solvent was removed in vacuo, the residue was subjected to preparative hplc and the required fraction dried by repetitive addition of acetonitrile and concentration under reduced pressure to give the title compound (0.020 g) as a colourless gum.

Aufarbeitung

  1. stirringThe reaction mixture was stirred at room temperature for 16 h
  2. customThe solvent was removed in vacuo
  3. dry with materialthe required fraction dried by repetitive addition of acetonitrile and concentration under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-035ef78554b34ae3b932c461930edf24
Quelldatensatz
uspto-grants-2001_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06326386B1

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