1-(2-ethoxyethyl)-3-ethyl-4-nitro-1H-pyrazole-5-carboxamide → 4-amino-1-(2-ethoxyethyl)-3-ethyl-1H-pyrazole-5-carboxamide

HRID 1896198

Reaktionsgleichung

Reaktionsgleichung von HRID 1896198
[CH2:1]([O:3][CH2:4][CH2:5][N:6]1[C:10]([C:11]([NH2:13])=[O:12])=[C:9]([N+:14]([O-])=O)[C:8]([CH2:17][CH3:18])=[N:7]1)[CH3:2].[H][H]>[Pt].C(OC(C)C)(=O)C>[NH2:14][C:9]1[C:8]([CH2:17][CH3:18])=[N:7][N:6]([CH2:5][CH2:4][O:3][CH2:1][CH3:2])[C:10]=1[C:11]([NH2:13])=[O:12]

Komponenten

5

Versuchsvorschrift

1-(2-ethoxyethyl)-3-ethyl-4-nitro-1H-pyrazole-5-carboxamide from step 1 (15.0 g, 58 mmol), 5% Platinum-on-carbon (0.75 g), and isopropyl acetate (150 mL) were combined and the mixture was stirred under 80 psi of hydrogen for about 50 hours. The mixture was then filtered through celite, the celite was rinsed with acetonitrile, and the filtrate was concentrated. The material eventually crystallized to give 13.7 g as a hydrate of the title compound.

Aufarbeitung

  1. filtrationThe mixture was then filtered through celite
  2. washthe celite was rinsed with acetonitrile
  3. concentrationthe filtrate was concentrated
  4. customThe material eventually crystallized

Quellen und Nachweise

ORD-Eintrag
ord-fe48cc5037154e5db3225d1bb8c24ee2
Quelldatensatz
uspto-grants-2013_08
Patentnummer
US08518956B2

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