Triethylamine → HCID 58786857, compound
Reaction equation
[C:1]([C:3]1([CH3:26])[CH2:8][N:7]([C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH2:6][CH2:5][N:4]1[C:16]([O:18][CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)=[O:17])#[N:2].CCN(CC)CC.[NH2:34][OH:35].Cl.[CH3:37][O:38][C:39]([C:41]#[C:42][C:43]([O:45][CH3:46])=[O:44])=[O:40]>CCO>[NH2:2]/[C:1](=[N:34]\[O:35]/[C:42](/[C:43]([O:45][CH3:46])=[O:44])=[CH:41]/[C:39]([O:38][CH3:37])=[O:40])/[C:3]1([CH3:26])[CH2:8][N:7]([C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH2:6][CH2:5][N:4]1[C:16]([O:18][CH2:19][C:20]1[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=1)=[O:17]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 40 °C
Procedure
A solution of 1-benzyl 4-tert-butyl 2-cyano-2-methylpiperazine-1,4-dicarboxylate (C-41) in EtOH was added to a solution of Et3N (3.2 eq) and NH2OH HCl (3 eq) in EtOH. The mixture was stirred 2 hr at 40° C. After evaporation of the solvent, the residue was diluted with AcOEt, washed with water, dried over Na2SO4, filtered and concentrated. The residue was further dissolved in chloroform and dimethylacetylenedicarboxylate (1.5 eq) added to the stirred solution. Reaction was refluxed over night. The mixture was evaporated and the residue was purified by flash chromatography on silica gel (petroleum ether/AcOEt, 65:35) affording (C-42).
Workup
- customAfter evaporation of the solvent
- additionthe residue was diluted with AcOEt
- washwashed with water
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated
- dissolutionThe residue was further dissolved in chloroform
- customReaction
- temperaturewas refluxed over night
- customThe mixture was evaporated
- customthe residue was purified by flash chromatography on silica gel (petroleum ether/AcOEt, 65:35)
- customaffording (C-42)
Sources & evidence
- ORD record
- ord-7267064be45942a89ed7d04b52bbcc79
- Source dataset
- uspto-grants-2008_12
- Patent number
- US07459452B2
Reaction notes
Loading…