Robinson, H; Oatley, SA; Rowedder, JE; Slade, P; Macdonald, SJF; Argent, SP; Hirst, JD; McInally, T; Moody, CJ in [Robinson, Henry; McInally, Thomas] Univ Nottingham, Sch Chem, GSK Carbon Neutral Labs Sustainable Chem, Jubilee Campus,Triumph Rd, Nottingham NG7 2TU, England; [Oatley, Steven A.; Argent, Stephen P.; Hirst, Jonathan D.; Moody, Christopher J.] Univ Nottingham, Sch Chem, Univ Pk, Nottingham NG7 2RD, England; [Rowedder, James E.; Slade, Pawel; Macdonald, Simon J. F.] GlaxoSmithKline Med Res Ctr, Med Sci & Technol, Gunnels Wood Rd, Stevenage SG1 2NY, Herts, England published Late-Stage Functionalization by Chan-Lam Amination: Rapid Access to Potent and Selective Integrin Inhibitors in 2020.0, Cited 39.0. Product Details of 67-51-6. The Name is 3,5-Dimethyl-1H-pyrazole. Through research, I have a further understanding and discovery of 67-51-6.
A late-stage functionalization of the aromatic ring in amino acid derivatives is described. The key step is a copper-catalysed diversification of a boronate ester by amination (Chan-Lam reaction) that can be carried out on a complex beta-aryl-beta-amino acid scaffold. This not only considerably extends the substrate scope of amination partners, but also delivers an array of potent and selective integrin inhibitors as potential treatment agents of idiopathic pulmonary fibrosis (IPF). This versatile chemical strategy, which is amenable to high-throughput-array protocols, allows the installation of pharmaceutically valuable heteroaromatic fragments at a late stage by direct coupling to NH heterocycles, leading to compounds with drug-like attributes. It thus constitutes a useful addition to the medicinal chemist’s repertoire.
Product Details of 67-51-6. About 3,5-Dimethyl-1H-pyrazole, If you have any questions, you can contact Robinson, H; Oatley, SA; Rowedder, JE; Slade, P; Macdonald, SJF; Argent, SP; Hirst, JD; McInally, T; Moody, CJ or concate me.
Reference:
Pyrazole – Wikipedia,
,Pyrazoles – an overview | ScienceDirect Topics