Dichloromethane → N-[2-(5-bromo-1-indolinyl)-5-bromophenyl]-4-methyl-1-piperazinecarboxamide

HRID 4036Notes

Reaction equation

HRID 4036 reaction equation
[Br:1]N1C(=O)CCC1=O.[N:9]1([C:18]2[CH:23]=[CH:22][C:21]([Br:24])=[CH:20][C:19]=2[NH:25][C:26]([N:28]2[CH2:33][CH2:32][N:31]([CH3:34])[CH2:30][CH2:29]2)=[O:27])[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH2:11][CH2:10]1.ClCCl>CN(C)C=O>[Br:1][C:14]1[CH:13]=[C:12]2[C:17](=[CH:16][CH:15]=1)[N:9]([C:18]1[CH:23]=[CH:22][C:21]([Br:24])=[CH:20][C:19]=1[NH:25][C:26]([N:28]1[CH2:29][CH2:30][N:31]([CH3:34])[CH2:32][CH2:33]1)=[O:27])[CH2:10][CH2:11]2

Participants

5

Reactant 3

HCID 6344DichloromethaneHCID 67184N-bromobutanimideHCID 13823352N-[2-(indolin-1-yl)-5-bromophenyl]-4-methyl-1-piperazinecarboxamide

Product 1

HCID 13823368N-[2-(5-bromo-1-indolinyl)-5-bromophenyl]-4-methyl-1-piperazinecarboxamideYield 84%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Conditions

Temperature
60 °C

Procedure

N-Bromosuccinimide (2.6 g, 14.5 mmoles) was added to a solution of N-[2-(indolin-1-yl)-5-bromophenyl]-4-methyl-1-piperazinecarboxamide (5.0 g, 12.0 mmoles) in dimethylformamide (50 ml). The solution was stirred at room temperature for 15 minutes and at 60° C. for 15 minutes. The solution was cooled and poured into dichloromethane (500 ml). The layers were separated and the organic phase was washed with water (3×500 ml), brine (500 ml), and dried over anhydrous sodium sulfate. The mixture was filtered and the filtrate was concentrated. The residue was purified by chromatography over silica gel (60 g, eluted with 4% methanol:96% dichloromethane, 1 l). The appropriate fractions were pooled and concentrated to give 4.8 g (84%) of product. Recrystallization from chloroform and hexane gave the analytical sample, mp 118°-119.5° C.

Workup

  1. temperatureThe solution was cooled
  2. customThe layers were separated
  3. washthe organic phase was washed with water (3×500 ml), brine (500 ml)
  4. dry with materialdried over anhydrous sodium sulfate
  5. filtrationThe mixture was filtered
  6. concentrationthe filtrate was concentrated
  7. customThe residue was purified by chromatography over silica gel (60 g, eluted with 4% methanol:96% dichloromethane, 1 l)
  8. concentrationconcentrated

Sources & evidence

ORD record
ord-53391d34fae14644b538478e4ff63a6d
Source dataset
uspto-grants-1988_02
Patent number
US04723007

Reaction notes

Loading…