Glycerol → 1,5-Naphthyridin-2-amine

HRID 868967Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 868967
[N:1]1[CH:6]=[C:5]([NH2:7])[CH:4]=[CH:3][C:2]=1[NH2:8].O[CH2:10][CH:11]([CH2:13]O)O.[N+](C1C=C(S([O-])(=O)=O)C=CC=1)([O-])=O.[Na+].S(=O)(=O)(O)O.[OH-].[Na+]>O>[N:1]1[C:6]2[C:5](=[N:7][CH:10]=[CH:11][CH:13]=2)[CH:4]=[CH:3][C:2]=1[NH2:8]

Komponenten

7

Reaktionsbedingungen

Temperatur
135 °C

Versuchsvorschrift

A mixture of pyridine-2,5-diamine (5.2 g, 71% pure, 33.9 mmol), glycerol (15.6 g, 169.5 mmol), sodium 3-nitrobenzenesulphonate (15.2 g, 67.8 mmol), sulfuric acid (20 mL), and water (30 mL) was heated to 135° C. and stirred at this temperature for 16 h. The mixture was cooled to room temperature and then poured into ice water (150 g). The pH of the reaction mixture was adjusted to 9 with saturated sodium hydroxide aqueous solution. Then the mixture was extracted with EtOAc (3×100 mL). The extracts were dried over sodium sulfate, concentrated under reduce pressure to give the crude product. The crude product was purified by column chromatography to give 2.0 g of 1,5-naphthyridin-2-amine as a yellow solid.

Aufarbeitung

  1. temperatureThe mixture was cooled to room temperature
  2. extractionThen the mixture was extracted with EtOAc (3×100 mL)
  3. dry with materialThe extracts were dried over sodium sulfate
  4. concentrationconcentrated
  5. customto give the crude product
  6. customThe crude product was purified by column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-3f57624f5d0f4e39b04916c3700b5cd7
Quelldatensatz
uspto-grants-2015_03
Patentnummer
US08969349B2

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