تفاعل #70040

ord-6cfc93dfe97b44509fdf6828efbfefa2

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
CN1CCN(c2ccc(C=O)cc2)CC1
4-(4-methylpiperazin-1-yl)benzaldehyde
CC(C)(C)[O-].[Na+]
sodium tert.-butoxide
CC(C)(C)OC(=O)CC(=O)[O-]
mono-tert-butyl malonate
CN1CCN(c2ccc(C3C(=O)CC(=O)N3c3ccc4[nH]cnc4c3)cc2)CC1
1-(1H-Benzo[d]imidazol-5-yl)-5-(4-(4-methylpiperazin-1-yl)phenyl)-pyrrolidine-2,4-dione

المذيبات

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 (0.85 mg, 6.37 mmol), 4-(4-methylpiperazin-1-yl)benzaldehyde (1.3 g, 6.37 mmol), mono-tert-butyl malonate (1.53 g, 9.55 mmol), 1-isocyano-2-methylpropan-2-yl methyl carbonate (1.1 g, 7.01 mmol) in MeOH/CH2Cl2 1:1 (30 ml) with stirring for 2.5 days and sodium tert.-butoxide (0.235 g, 2.10 mmol) according to method 5.

المصدر

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