2-(6-bromo-1H-benzimidazol-2-yl)pyrrolidine-1-carboxylic acid tert-butyl ester → 6-Bromo-2-pyrrolidin-2-yl-1H-benzoimidazole
Reaction equation
COC(=O)NC(C(N1CCCC1C1NC(C2C=CC(Br)=CC=2)=CN=1)=O)C(C)C.C(OC([N:36]1[CH2:40][CH2:39][CH2:38][CH:37]1[C:41]1[NH:45][C:44]2[CH:46]=[C:47]([Br:50])[CH:48]=[CH:49][C:43]=2[N:42]=1)=O)(C)(C)C>>[Br:50][C:47]1[CH:48]=[CH:49][C:43]2[N:42]=[C:41]([CH:37]3[CH2:38][CH2:39][CH2:40][NH:36]3)[NH:45][C:44]=2[CH:46]=1Participants
3
Procedure
Prepared by the same method as (1-{2-[5-(4-Bromo-phenyl)-1H-imidazol-2-yl]-pyrrolidine-1-carbonyl}-2-methyl-propyl)-carbamic acid methyl ester, except that 2-(6-Bromo-1H-benzoimidazol-2-yl)-pyrrolidine-1-carboxylic acid tert-butyl ester was used as the substrate. 120 mg light yellow solid (66% yield).