3-oxopentanenitrile → 5-Ethyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine

HRID 1042073Notes

Reaction equation

HRID 1042073 reaction equation
O=[C:2]([CH2:6][CH3:7])[CH2:3][C:4]#[N:5].[NH2:8][C:9]1[N:13]=[CH:12][NH:11][N:10]=1>C(O)(=O)C>[CH2:6]([C:2]1[CH:3]=[C:4]([NH2:5])[N:10]2[N:11]=[CH:12][N:13]=[C:9]2[N:8]=1)[CH3:7]

Participants

4

Conditions

Temperature
150 °C

Procedure

A mixture of 3-oxopentanenitrile (1.0 g, 10.3 mmol) and 3-amino-1,2,4-triazole (0.91 g, 10.8 mmol) in 10 mL of acetic acid was heated in a pressure tube at 150° C. for 24 h. The reaction mixture was allowed to cool to room temperature, and solvent was removed in vacuo. The solid was removed via filtration. The filtrate partially upon standing at room temperature, and the solid was collected via filtration to give the title compound (200 mg, 12% yield).

Workup

  1. temperatureto cool to room temperature
  2. customsolvent was removed in vacuo
  3. customThe solid was removed via filtration
  4. customupon standing at room temperature
  5. filtrationthe solid was collected via filtration

Sources & evidence

ORD record
ord-683cdf2c034c415a956c712c2a4b91ec
Source dataset
uspto-grants-2013_10
Patent number
US08557828B2

Reaction notes

Loading…