Triethylamine → N-[4-(3-chloro-5-trifluoromethyl-2-pyridyloxy)benzyl]-4-chloro-3-ethyl-1-methyl-5-pyrazolecarboxamide

HRID 2248378

Reaktionsgleichung

Reaktionsgleichung von HRID 2248378
C(OCC)(=O)C.[Cl:7][C:8]1[C:9]([O:18][C:19]2[CH:26]=[CH:25][C:22]([CH2:23][NH2:24])=[CH:21][CH:20]=2)=[N:10][CH:11]=[C:12]([C:14]([F:17])([F:16])[F:15])[CH:13]=1.C(N(CC)CC)C.CC1C=CC(OC2C=CC(CN[C:46]([C:48]3[N:52]([CH3:53])[N:51]=[C:50]([CH2:54][CH3:55])[C:49]=3[Cl:56])=[O:47])=CC=2)=CC=1>O>[Cl:7][C:8]1[C:9]([O:18][C:19]2[CH:26]=[CH:25][C:22]([CH2:23][NH:24][C:46]([C:48]3[N:52]([CH3:53])[N:51]=[C:50]([CH2:54][CH3:55])[C:49]=3[Cl:56])=[O:47])=[CH:21][CH:20]=2)=[N:10][CH:11]=[C:12]([C:14]([F:17])([F:15])[F:16])[CH:13]=1

Komponenten

6

Edukt 4

HCID 8471TriethylamineHCID 8857Ethyl AcetateHCID 10110536TolfenpyradHCID 199960544-(3-Chloro-5-trifluoromethyl-2-pyridyloxy)benzylamine

Produkt 1

HCID 19996056N-[4-(3-chloro-5-trifluoromethyl-2-pyridyloxy)benzyl]-4-chloro-3-ethyl-1-methyl-5-pyrazolecarboxamide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

Into 50 ml solution of ethyl acetate containing 2.49 g of 4-(3-chloro-5-trifluoromethyl-2-pyridyloxy)benzylamine and 1.21 g of triethylamine, was dropped 2.07 g of 4-chloro-3-ethyl-1-methyl-5-pyrazolecarboxylic acid chloride synthesized in Example 2. After the completion of dropping, the mixture was stirred for 1 hour, poured into iced water and then extracted with ethyl acetate. The ethyl acetate layer was washed with an aqueous solution of sodium carbonate, water and a saturated aqueous solution of sodium chloride. After drying over anhydrous sodium sulfate, the solution was concentrated under a reduced pressure. The residue was purified on silica gel column chromatography to obtain 3.35 g of the titled compound (No. 75) shown in Table 1.

Aufarbeitung

  1. extractionextracted with ethyl acetate
  2. washThe ethyl acetate layer was washed with an aqueous solution of sodium carbonate, water
  3. dry with materialAfter drying over anhydrous sodium sulfate
  4. concentrationthe solution was concentrated under a reduced pressure
  5. customThe residue was purified on silica gel column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-d3455af18c8646cb817ae64a32cf5282
Quelldatensatz
uspto-grants-1991_08
Patentnummer
US05039693

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