New downstream synthetic route of 91912-53-7

In addition to the literature in the link below, there is a lot of literature about this compound(3-(Pyridin-4-yl)-1H-pyrazol-5-amine)Product Details of 91912-53-7, illustrating the importance and wide applicability of this compound(91912-53-7).

The reaction of an aromatic heterocycle with a proton is called a protonation. One of articles about this theory is 《Novel pyrazolopyrimidines as highly potent B-Raf inhibitors》. Authors are Di Grandi, Martin J.; Berger, Dan M.; Hopper, Darrin W.; Zhang, Chunchun; Dutia, Minu; Dunnick, Alejandro L.; Torres, Nancy; Levin, Jeremy I.; Diamantidis, George; Zapf, Christoph W.; Bloom, Jonathan D.; Hu, YongBo; Powell, Dennis; Wojciechowicz, Donald; Collins, Karen; Frommer, Eileen.The article about the compound:3-(Pyridin-4-yl)-1H-pyrazol-5-aminecas:91912-53-7,SMILESS:NC1=CC(C2=CC=NC=C2)=NN1).Product Details of 91912-53-7. Through the article, more information about this compound (cas:91912-53-7) is conveyed.

A novel series of pyrazolo[1,5-a]pyrimidines bearing a 3-hydroxyphenyl group at C(3) and substituted tropanes at C(7) have been identified as potent B-Raf inhibitors. Exploration of alternative functional groups as a replacement for the C(3) phenol demonstrated indazole to be an effective isostere. Several compounds possessing substituted indazole residues, such as 4e, 4p, and 4r, potently inhibited cell proliferation at submicromolar concentrations in the A375 and WM266 cell lines, and the latter two compounds also exhibited good therapeutic indexes in cells.

In addition to the literature in the link below, there is a lot of literature about this compound(3-(Pyridin-4-yl)-1H-pyrazol-5-amine)Product Details of 91912-53-7, illustrating the importance and wide applicability of this compound(91912-53-7).

Reference:
Pyrazine – Wikipedia,
Pyrazine | C4H4N2 – PubChem