تفاعل #1511353

ord-940e6bbb6e86463baa1a7407ecb14986

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزThe reaction mixture was concentrated in vacuo
  2. 2
    أخرىpurified by SCX-2 cartridge (16 mg, 72%)

الإجراء التجريبي

The title compound was prepared according to Method 4 using (4R,5R)-3-(tert-butoxycarbonyl)-2,2,5-trimethyl-1,3-oxazolidine-4-carboxylic acid (Preparation 59A) and 3′,4′-diaminobiphenyl-4-carbonitrile (Preparation 82). The reaction mixture was concentrated in vacuo and purified by SCX-2 cartridge (16 mg, 72%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08927587B2uspto-grants-2015_01