2,4-Difluoroaniline → HCID 22013907, Verbindung

HRID 2416953Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2416953
CCN=C=NCCCN(C)C.C1C=CC2N(O)N=NC=2C=1.[F:22][C:23]1[CH:29]=[C:28]([F:30])[CH:27]=[CH:26][C:24]=1[NH2:25].[Br:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][C:41](O)=[O:42]>CN(C=O)C>[Br:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][C:41]([NH:25][C:24]1[CH:26]=[CH:27][C:28]([F:30])=[CH:29][C:23]=1[F:22])=[O:42]

Komponenten

6

Versuchsvorschrift

WSC (990 mg, 5.2 mmols) and HOBt (698 mg, 5.2 mmols) were added to a DMF (10 ml) solution of 2,4-difluoroaniline (1.29 g, 10 mmols) and 10-bromodecanoic acid (1.18 g, 4.7 mmols), and stirred at room temperature for 15 hours. The reaction mixture was extracted with ether. The organic layer was washed with water, 1 N HCl an aqueous saturated solution of sodium hydrogencarbonate and saturated saline in that order, and dried with anhydrous magnesium sulfate, and the solvent was evaporated. Then, the residue was purified through silica gel column chromatography (developer:hexane/acetone=10/1) aid the resulting crystals were recrystallized from ether-hexane to obtain 763 mg (yield, 45%) of 10-bromo-N-(2,4-difluorophenyl) decanamide as colorless needle-like crystals.

Aufarbeitung

  1. extractionThe reaction mixture was extracted with ether
  2. washThe organic layer was washed with water, 1 N HCl an aqueous saturated solution of sodium hydrogencarbonate and saturated saline in that order
  3. dry with materialdried with anhydrous magnesium sulfate
  4. customthe solvent was evaporated
  5. customThen, the residue was purified through silica gel column chromatography (developer:hexane/acetone=10/1) aid the resulting crystals
  6. customwere recrystallized from ether-hexane

Quellen und Nachweise

ORD-Eintrag
ord-5c1d70fff51d452e8fea49b87e66351a
Quelldatensatz
uspto-grants-2004_11
Patentnummer
US06825223B2

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