e.g. Filippa Pettersson or Cancer Res. 75(6) , 1102-12, (2015) or 10.1002/anie.201600521
Tetrahedron
Process development of a disease-modifying antirheumatic drug, TAK-603, based on optimization of Friedel–Crafts reaction and selective substitution of a triazole ring
M Mizuno, A Inagaki, M Yamashita, N Soma, Y Maeda…
A practical method for the preparation of, an antirheumatic drug, has been developed. As a result of optimizing the Friedel–Crafts reaction in the presence of SnCl4/POCl3, 2- aminobenzophenone skeleton, the key intermediate of, was formed with good yield. The selective substitution reaction of 1, 2, 4-triazole was accomplished using 4-amino-1, 2, 4- triazole and deamination.