1-Isopropylhydrazine → 5-amino-1-(propan-2-yl)-1H-pyrazole-4-carboxylic acid

HRID 475937

Reaktionsgleichung

Reaktionsgleichung von HRID 475937
[C:1](/[C:3](=[CH:9]/OCC)/[C:4]([O:6]CC)=[O:5])#[N:2].[CH:13]([NH:16][NH2:17])([CH3:15])[CH3:14]>C(O)C>[NH2:2][C:1]1[N:16]([CH:13]([CH3:15])[CH3:14])[N:17]=[CH:9][C:3]=1[C:4]([OH:6])=[O:5]

Komponenten

4

Versuchsvorschrift

To a solution of ethyl (2Z)-2-cyano-3-(ethyloxy)-2-propenoate (114.2 g, 0.67 mol) in ethanol (250 mL) was slowly added isopropylhydrazine (55 g, 0.74 mol) in a dropwise manner. The mixture was heated at reflux for 4 h, and then cooled to room temperature. The mixture was concentrated in vacuo. Approximately half of the crude 5-amino-1-isopropyl-1H-pyrazole-4-carboxylic acid ethyl ester (50 g) was suspended in an aqueous solution of sodium hydroxide (4M, 130 mL), and stirred with heating at reflux for 2 h. The reaction mixture was then cooled to room temperature and adjusted to pH=3.5 with concentrated HCl, wherein precipitate formation ensued. The solid was collected by filtration and dried in vacuum oven overnight to afford crude 5-amino-1-isopropyl-1H-pyrazole-4-carboxylic acid (30 g). The solid was suspended in diphenyl ether (120 mL) and stirred with heating at 160-165° C. for 2 h. The solution was then cooled to room temperature and the solvent removed in vacuo. The crude product was purified by silica gel chromatography (eluent: petroleum ether/EtOAc=1:1) to afford the product as 12 g. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.24 (d, 6H, J=6.4 Hz), 4.32 (m, 1H), 5.06 (s, 2H), 5.21 (s, 1H), 7.00 (s, 1H).

Aufarbeitung

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 4 h
  3. concentrationThe mixture was concentrated in vacuo
  4. temperaturewith heating
  5. temperatureat reflux for 2 h
  6. temperatureThe reaction mixture was then cooled to room temperature
  7. filtrationThe solid was collected by filtration
  8. customdried in vacuum oven overnight

Quellen und Nachweise

ORD-Eintrag
ord-ef79bc0041c94454a94a01f8d090e033
Quelldatensatz
uspto-grants-2014_01
Patentnummer
US08637509B2

Verknüpfte Notizen

Wird geladen…