The important role of 5-Amino-4H-1,2,4-triazole-3-carboxylic acid

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route 3641-13-2, its application will become more common.

Some common heterocyclic compound, 3641-13-2, name is 5-Amino-4H-1,2,4-triazole-3-carboxylic acid, molecular formula is C3H4N4O2, traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route. Application In Synthesis of 5-Amino-4H-1,2,4-triazole-3-carboxylic acid

3-Amino-1,2,4-triazole-5-carboxylic acid hydrate (1.28g, O.OImol) was dissolved in water (50ml). Sodium nitrite (0.76g, 0.011mol) was added and the solution was stirred until the sodium nitrite had dissolved. The mixture was then added dropwise to a cooled mix of ice-water (30g) and concentrated hydrochloric acid (3.0ml) at 0-5C. The mixture was stirred for 30 minutes at 0-5C and then excess nitrous acid was destroyed by the addition of sulfamic acid. The resultant diazonium salt suspension was added slowly to a solution of 6-hydroxyquinoline (1.45g, O.OImol) in water (100ml) at pH 8-9 (adjusted with 2M NaOH) and cooled to below 5C. The reaction mixture was then stirred at 0-5C for one hour and the product was precipitated by acidification to pH 4 with 2M HCI and collected by filtration. The product was washed with water and then dried in a vacuumdesiccator to give an orange solid.

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route 3641-13-2, its application will become more common.

Reference:
Patent; AVECIA LIMITED; WO2004/108834; (2004); A2;,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics