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Water → HCID 59676872, Verbindung

HRID 902890
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 902890
O.[OH-].[Li+:3].[Cl:4][C:5]1[CH:6]=[CH:7][C:8]([NH:11][C:12](=[O:17])[C:13]([O:15]C)=[O:14])=[N:9][CH:10]=1>O1CCCC1>[Cl:4][C:5]1[CH:6]=[CH:7][C:8]([NH:11][C:12](=[O:17])[C:13]([O-:15])=[O:14])=[N:9][CH:10]=1.[Li+:3]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 962WaterHCID 3939Lithium HydroxideHCID 44119563Methyl [(5-chloropyridin-2-yl)amino](oxo)acetate

Produkt 1

HCID 59676872HCID 59676872, VerbindungAusbeute 102,6 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

Methyl chlorooxoacetate (78.7 ml) was added dropwise to a suspension of 2-amino-5-chloropyridine (100 g) and sodium hydrogencarbonate (78.4 g) in tetrahydrofuran (2000 ml) at 0° C., and the mixture was stirred at room temperature for 2 hours. After the reaction mixture was added to a mixture of diethyl ether (2000 ml), ammonium chloride (62.4 g) and water (1000 ml), liquid separation was performed. The resultant water layer was extracted with methylene chloride. Organic layers were combined and dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure to obtain methyl 2-[(5-chloropyridin-2-yl)amino]-2-oxoacetate (162 g). Water (450 ml) and lithium hydroxide (18.2 g) were added to a solution of this ester (160 g) in tetrahydrofuran (1800 ml). After the mixture was stirred at room temperature for 2 hours, the solvent was distilled off under reduced pressure, and hexane (3000 ml) was added to the resultant residue to stir the mixture for 3 hours. Solids were collected by filtration and dried. Acetonitrile (1000 ml) was added to the solids (190 g), and the mixture was stirred for 1 hour. Solids formed were collected by filtration, washed with diethyl ether (500 ml) and then dried to obtain the title compound (158 g).

Aufarbeitung

  1. distillationthe solvent was distilled off under reduced pressure, and hexane (3000 ml)
  2. additionwas added to the resultant residue
  3. stirringto stir the mixture for 3 hours
  4. filtrationSolids were collected by filtration
  5. customdried
  6. additionAcetonitrile (1000 ml) was added to the solids (190 g)
  7. stirringthe mixture was stirred for 1 hour
  8. customSolids formed
  9. filtrationwere collected by filtration
  10. washwashed with diethyl ether (500 ml)
  11. customdried

Quellen und Nachweise

ORD-Eintrag
ord-444bb24853ea49d7839744a64c302c16
Quelldatensatz
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07365205B2

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