Hydrochloric Acid → HCID 57642851, Verbindung

HRID 501439Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 501439
Cl.[CH2:2]([NH:5][C:6]1[CH:11]=[CH:10][N:9]=[CH:8][C:7]=1[N+:12]([O-])=O)[CH:3]=[CH2:4].[Sn](Cl)(Cl)(Cl)[Cl:16]>>[CH2:2]([NH:5][C:6]1[CH:11]=[CH:10][N:9]=[C:8]([Cl:16])[C:7]=1[NH2:12])[CH:3]=[CH2:4]

Komponenten

4

Reaktionsbedingungen

Temperatur
90 °C

Versuchsvorschrift

55 ml of 35% hydrochloric acid was added to 3.02 g of allyl-(3-nitropyridin-4-yl)amine, and the mixture was heated to 90° C. 19.1 g of tin chloride was added to the solution, and the mixture was kept at 90° C. for 30 minutes. The reaction solution was cooled in an ice-water bath, and then 250 ml ice/water was added thereto. The reaction solution was concentrated under reduced pressure, and then 250 ml of ammonia-saturated methanol was added thereto. The mixture was stirred for 20 hours. 750 ml of ethyl acetate was added to the solution, and the mixture was filtered through celite. The filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography. Thus, 2.88 g of the title compound was obtained from the fraction eluted with ethyl acetate-hexane (1:1).

Aufarbeitung

  1. temperatureThe reaction solution was cooled in an ice-water bath
  2. concentrationThe reaction solution was concentrated under reduced pressure
  3. addition250 ml of ammonia-saturated methanol was added
  4. addition750 ml of ethyl acetate was added to the solution
  5. filtrationthe mixture was filtered through celite
  6. concentrationThe filtrate was concentrated under reduced pressure
  7. customThe residue was purified by silica gel column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-9c13a56b5ba44ea2b61999d2929b8fb9
Quelldatensatz
uspto-grants-2010_08
Patentnummer
US07772226B2

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