تفاعل #70037

ord-2e7227c23df247d9a6549863a438121f

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(C2CCOCC2)cc1
4-(tetrahydro-2H-pyran-4-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(C2CCOCC2)cc1
1-(1H-Benzo[d]imidazol-5-yl)-5-(4-(tetrahydro-2H-pyran-4-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 (1.04 g, 7.89 mmol), 4-(tetrahydro-2H-pyran-4-yl)benzaldehyde (1.0 g, 5.26 mmol), mono-tert-butyl malonate (0.84 g, 5.26 mmol), 1-isocyano-2-methylpropan-2-yl methyl carbonate (0.83 g, 5.26 mmol) and sodium tert.-butoxide (0.829 g, 7.39 mmol) according to method 5.

المصدر

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