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2,3-Diaminopyridine → HCID 178448403, Verbindung

HRID 2054443
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2054443
[NH2:1][C:2]1[C:7]([NH2:8])=[CH:6][CH:5]=[CH:4][N:3]=1.[Cl:9][CH:10]([CH2:14][CH3:15])[C:11](O)=O>O>[Cl:9][CH:10]([C:11]1[NH:1][C:2]2=[N:3][CH:4]=[CH:5][CH:6]=[C:7]2[N:8]=1)[CH2:14][CH3:15]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 99562,3-DiaminopyridineHCID 201372-Chlorobutyric acid

Produkt 1

HCID 178448403HCID 178448403, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

5.0 g of 2,3-diaminopyridine in 200 g of polyphosphoric acid are heated at 120° C. for 0.5 h. The solution is cooled to 80° C. and 5.7 ml of 2-chlorobutyric acid are added. Thereafter, the reaction mixture is heated to 130° C. for 22 h. After cooling, the polyphosphoric acid is hydrolysed with water, the mixture is filtered using charcoal and celite and the pH value of the filtrate is adjusted to pH 4 using 9 M aqueous sodium hydroxide solution. The mixture is extracted three times each with 200 ml of ethyl acetate, the combined organic phases are dried using sodium sulfate, concentrated and the residue is purified by chromatography on silica gel (eluent: toluene/ethyl acetate 1:1) to give 5.19 g of the title compound as a colorless, amorpheous solid. M.p. 137° C. TLC: Rf=0.50 (dichloromethane/methanol 10:1).

Aufarbeitung

  1. temperatureThereafter, the reaction mixture is heated to 130° C. for 22 h
  2. temperatureAfter cooling
  3. filtrationthe mixture is filtered
  4. extractionThe mixture is extracted three times each with 200 ml of ethyl acetate
  5. customthe combined organic phases are dried
  6. concentrationconcentrated
  7. customthe residue is purified by chromatography on silica gel (eluent: toluene/ethyl acetate 1:1)

Quellen und Nachweise

ORD-Eintrag
ord-accb37b4f26e4bf2999888ef5285ad22
Quelldatensatz
uspto-grants-2008_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07329677B2

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