Continuously updated synthesis method about 5-Methyl-4H-1,2,4-triazol-3-amine

In conclusion, we affirm that quantitative kinetic descriptions of catalytic behavior continue to serve as an indispensable tool to navigate research efforts intended to model. Read on for other articles about 4923-01-7.

Research speed reading in 2021. The prevalence of solvent effects in heterogeneous catalysis in condensed media has motivated developing quantitative kinetic. 4923-01-7, name is 5-Methyl-4H-1,2,4-triazol-3-amine belongs to triazoles compound, it is a common compound, a new synthetic route is introduced below. Application In Synthesis of 5-Methyl-4H-1,2,4-triazol-3-amine

A mixture of methyl 3-oxo-2-(4-(4-(trifluoromethoxy)phenyl)piperidin-1 -yl)butanoate (46A) (300 mg, 0.835 mmol) and 3-methyl-1 H-1 ,2,4-triazol-5-am ine (123 mg, 1 .252 mmol) in acetic acid (10 mL) was heated at 130 C for 2 h . Then reaction mixture was diluted with water (20 mL), adjusted to pH=6 by addition of saturated Na2C03 solution and extracted with EtOAc twice. Organic layers were combined, dried over Na2S04 and concentrated to give a crude product, which was purified by ISCO with 0-1 00% EtOAc:EtOH (3:1 ) in hexanes to give two peaks of same mass. Peak two was the desired product based on NMR. 1 H NMR (400 MHz, DMSO-d6) delta 7.48 – 7.40 (m , 2H), 7.30 (dt, J = 7.8, 1 .1 Hz, 2H) , 3.49 (t, J = 11 .4 Hz, 2H), 2.87 – 2.74 (m , 2H), 2.74 – 2.60 (m , 1 H), 2.41 (s, 3H), 2.34 (s, 3H), 1 .87 – 1 .63 (m , 4H). Method 1 : RT = 1 .12 min. ; M/Z (M+H) = 408.1 .

In conclusion, we affirm that quantitative kinetic descriptions of catalytic behavior continue to serve as an indispensable tool to navigate research efforts intended to model. Read on for other articles about 4923-01-7.

Reference:
Patent; NOVARTIS AG; CHIANELLI, Donatella; GIBNEY, Michael; LERARIO, Isabelle K.; LIANG, Fang; LIU, Xiaodong; MOLTENI, Valentina; NAGLE, Advait Suresh; SMITH, Jeffrey M.; SUPEK, Frantisek; XIE, Yongping; YEH, Vince; (64 pag.)WO2018/229683; (2018); A1;,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics