1-Methylpiperazine → HCID 18321587, compound

HRID 1782741Notes

Reaction equation

HRID 1782741 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

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

  1. additionwas added dropwise at room temperature within 30 minutes
  2. filtrationinsoluble matter was filtered off
  3. customthe filtrate evaporated down in vacuo
  4. customAfter purification of the raw product on silica gel (Amicon, 35-70 μm)
  5. washammonia(80/20/1 v/v/v) for elution, 700 mg (22% of theory) of colourless crystals
  6. customwere obtained of Mp. 130° C.

Sources & evidence

ORD record
ord-0794e5dbfbc54addb76c727c8bea4fd9
Source dataset
uspto-grants-2009_03
Patent number
US07498325B2

Reaction notes

Loading…