Potassium Hydroxide → 5-Hydrazinyl-2-methoxypyridine

HRID 431047

Reaktionsgleichung

Reaktionsgleichung von HRID 431047
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([O:8][CH3:9])=[N:6][CH:7]=1.[N:10]([O-])=O.[Na+].O.O.[Sn](Cl)Cl.[OH-].[K+]>Cl.O.C(OCC)C>[NH:1]([C:2]1[CH:3]=[CH:4][C:5]([O:8][CH3:9])=[N:6][CH:7]=1)[NH2:10]

Komponenten

8

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

5-Amino-2-methoxypyridine (5.0 g, 40 mmol) was dissolved in 6 N HCl (10 mL), cooled to 0° C., and vigorously stirred throughout the procedure. Sodium nitrite (2.8 g, 41 mmol) was dissolved in water (10 mL) and this solution was added to the reaction solution. After 30 min, tin (II) chloride dihydrate (52 g, 230 mmol) in 6 N HCl (20 mL) was added, and the reaction slurry was stirred at 0° C. for 2.5 h. The pH was adjusted to 13 with 40% aqueous potassium hydroxide solution. Ethyl ether was added and the mixture was extracted with EtOAc (4×70 mL), dried (MgSO4) and concentrated to give 5-hydrazino-2-methoxypyridine as an orange solid (5.1 g).

Aufarbeitung

  1. additionthis solution was added to the reaction solution
  2. stirringthe reaction slurry was stirred at 0° C. for 2.5 h
  3. extractionthe mixture was extracted with EtOAc (4×70 mL)
  4. dry with materialdried (MgSO4)
  5. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-64e9bbe8871d426f8a4e0cc02f8f16bb
Quelldatensatz
uspto-grants-2003_12
Patentnummer
US06656933B2

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