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Putrescine → 6-[(4-Aminobutyl)amino]-3-pyridinecarbonitrile

HRID 2281965
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2281965
Cl[C:2]1[N:7]=[CH:6][C:5]([C:8]#[N:9])=[CH:4][CH:3]=1.[NH2:10][CH2:11][CH2:12][CH2:13][CH2:14][NH2:15]>>[NH2:10][CH2:11][CH2:12][CH2:13][CH2:14][NH:15][C:2]1[N:7]=[CH:6][C:5]([C:8]#[N:9])=[CH:4][CH:3]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 1045PutrescineHCID 51520946-Chloro-3-pyridinecarbonitrile

Produkt 1

HCID 570445896-[(4-Aminobutyl)amino]-3-pyridinecarbonitrile

Reaktionsbedingungen

Temperatur
170 °C

Versuchsvorschrift

6-Chloro-3-pyridinecarbonitrile (5.0 g) was dissolved in 1,4-diaminobutane (50 ml), and the solution was stirred at 170° C. for 2 hours with heating. Diethyl ether and distilled water were added to the reaction mixture, the layers were separated, and the aqueous layer was extracted with diethyl ether. The aqueous layer was saturated with sodium chloride, and the resulting mixture was extracted with chloroform. The resulting organic layer was dried over anhydrous magnesium sulfate, and filtered, and the filtrate was concentrated under reduced pressure to obtain the title compound (4.77 g).

Aufarbeitung

  1. temperaturewith heating
  2. distillationDiethyl ether and distilled water
  3. additionwere added to the reaction mixture
  4. customthe layers were separated
  5. extractionthe aqueous layer was extracted with diethyl ether
  6. extractionthe resulting mixture was extracted with chloroform
  7. dry with materialThe resulting organic layer was dried over anhydrous magnesium sulfate
  8. filtrationfiltered
  9. concentrationthe filtrate was concentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-d55adc20c14845db9834123deff5324f
Quelldatensatz
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09139609B2

Notizen zur Reaktion

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