تفاعل #70042

ord-84d2db6385904b519ccf9fce77940e80

معادلة التفاعل

[C-]#[N+]CC(C)(C)OC(=O)OC
1-isocyano-2-methylpropan-2-yl methyl carbonate
Nc1ccc2[nH]cnc2c1
1H-benzo[d]imidazol-5-amine
O=Cc1ccc(N2CCC(O)CC2)cc1
4-(4-hydroxypiperidin-1-yl)benzaldehyde
CC(C)(C)[O-].[Na+]
sodium tert.-butoxide
CC(C)(C)OC(=O)CC(=O)[O-]
mono-tert-butyl malonate
O=C1CC(=O)N(c2ccc3[nH]cnc3c2)C1c1ccc(N2CCC(O)CC2)cc1
1-(1H-Benzo[d]imidazol-5-yl)-5-(4-(4-hydroxypiperidin-1-yl)phenyl)-pyrrolidine-2,4-dione

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe compound was synthesized

الإجراء التجريبي

The compound was synthesized starting from 1H-benzo[d]imidazol-5-amine (0.970 g, 7.3 mmol), 4-(4-hydroxypiperidin-1-yl)benzaldehyde (1.5 g, 7.3 mmol), mono-tert-butyl malonate (1.17 g, 7.3 mmol), 1-isocyano-2-methylpropan-2-yl methyl carbonate (1.15 g, 7.3 mmol) and sodium tert.-butoxide (1.5 g, 14.6 mmol) according to method 5.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08530670B2uspto-grants-2013_09