1-Methylpiperazine → HCID 18321587, compound
Reaction equation
ClC(Cl)(O[C:5](=[O:11])OC(Cl)(Cl)Cl)Cl.[CH3:13][N:14]1[CH2:19][CH2:18][NH:17][CH2:16][CH2:15]1.CCN(C(C)C)C(C)C.[CH3:29][C:30]([CH3:41])([O:32][C:33]([N:35]1[CH2:40][CH2:39][NH:38][CH2:37][CH2:36]1)=[O:34])[CH3:31]>ClCCl>[CH3:31][C:30]([CH3:41])([O:32][C:33]([N:35]1[CH2:36][CH2:37][N:38]([C:5]([N:17]2[CH2:18][CH2:19][N:14]([CH3:13])[CH2:15][CH2:16]2)=[O:11])[CH2:39][CH2:40]1)=[O:34])[CH3:29]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 1.1 g of triphosgene (3.7 mMol) in 20 ml of dichloromethane, a mixture of 1.2 g (10 mMol) of 1-methyl-piperazine, 0.38 ml (22 mMol) of DIEA and 35 ml of dichloromethane was added dropwise at room temperature within 30 minutes, and then the solution of 1.9 g (10 mMol) of 1-(1,1-dimethyl-ethoxycarbonyl)piperazine and 0.38 ml of DIEA in 20 ml dichloromethane were added. After stirring for an hour at room temperature, insoluble matter was filtered off and the filtrate evaporated down in vacuo. After purification of the raw product on silica gel (Amicon, 35-70 μm), using dichloromethane/methanol/conc. ammonia(80/20/1 v/v/v) for elution, 700 mg (22% of theory) of colourless crystals were obtained of Mp. 130° C.
Workup
- additionwas added dropwise at room temperature within 30 minutes
- filtrationinsoluble matter was filtered off
- customthe filtrate evaporated down in vacuo
- customAfter purification of the raw product on silica gel (Amicon, 35-70 μm)
- washammonia(80/20/1 v/v/v) for elution, 700 mg (22% of theory) of colourless crystals
- customwere obtained of Mp. 130° C.
Sources & evidence
- ORD record
- ord-0794e5dbfbc54addb76c727c8bea4fd9
- Source dataset
- uspto-grants-2009_03
- Patent number
- US07498325B2
Reaction notes
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