Analyzing the synthesis route of 1001401-62-2

The synthetic route of 1001401-62-2 has been constantly updated, and we look forward to future research findings.

In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. 1001401-62-2, name is 2-(2H-1,2,3-Triazol-2-yl)benzoic acid belongs to Triazoles compound, it is a common compound, a new synthetic route is introduced below. Recommanded Product: 1001401-62-2

A solution of 2-(2H-1,2,3-triazol-2-yl)benzoic acid (P. Coleman, J. Schreier, WO2007/126934) (1 g, 4.1 mmol) in SOCl2 (10 mL) was stirred at 80 C for 30 min. The solvent was removed under reduced pressure and toluene (10 mL) was added to give solution A. The product from step 4 (1 g, 4.1 mmol) was dissolved in DCM (10 mL), DIEA (1.58 g, 12 mmol) added, and then solution A added at 0 C. The resulting mixture was stirred at RT for 2 h, then poured into water (10 mL) and extracted with DCM (10 mL x 3). The combined organic layers were washed with brine (10 mL), dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified by chromatography on silica (petroleum ether : EtOAc = 10 : 1 to = 3 : 1) then purified by prep. TLC (petroleum ether : EtOAc = 1 : 1) to give the title compound (0.2 g). LRMS m/z (Mu+Eta) 416.0, 418.0 found, 416.1, 418.1 required.

The synthetic route of 1001401-62-2 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; MERCK SHARP & DOHME CORP.; LIVERTON, Nigel; BESHORE, Douglas, C.; KUDUK, Scott, D.; LUO, Yunfu; MENG, Na; YU, Tingting; WO2015/20930; (2015); A1;,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics