N,N-Dimethylethylenediamine → 4-(3,4-Dichlorophenyl)-N-[2-(dimethylamino)ethyl]-1-piperazinecarboxamide

HRID 1087829Notes

Reaction equation

HRID 1087829 reaction equation
[CH3:1][N:2]([CH3:21])[CH2:3][CH2:4][NH:5][C:6](N1CCN(C2C=CC(F)=CC=2)CC1)=[O:7].C(N1C=CN=C1)(N1C=CN=C1)=O.CN(CCN)C.[Cl:40][C:41]1[CH:42]=[C:43]([N:48]2[CH2:53][CH2:52][NH:51][CH2:50][CH2:49]2)[CH:44]=[CH:45][C:46]=1[Cl:47]>O1CCCC1>[Cl:40][C:41]1[CH:42]=[C:43]([N:48]2[CH2:53][CH2:52][N:51]([C:6]([NH:5][CH2:4][CH2:3][N:2]([CH3:21])[CH3:1])=[O:7])[CH2:50][CH2:49]2)[CH:44]=[CH:45][C:46]=1[Cl:47]

Participants

6

Reactant 4

HCID 66053N,N-DimethylethylenediamineHCID 682631,1'-CarbonyldiimidazoleHCID 936011-(3,4-Dichlorophenyl)piperazineHCID 14763463N-[2-(Dimethylamino)ethyl]-4-(4-fluorophenyl)-1-piperazinecarboxamide

Product 1

HCID 147634864-(3,4-Dichlorophenyl)-N-[2-(dimethylamino)ethyl]-1-piperazinecarboxamide

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

This compound was prepared according to the procedure used to synthesize the compound of Example 11. A mixture of 2.5 g (0.025 mole) of 1,1'-carbonyldiimidazole, 1.4 g (0.015 mole) of unsym-dimethylethylenediamine and 3.6 g (0.015 mole) of 1-(3,4-dichlorophenyl)piperazine in a total of 100 ml of tetrahydrofuran gave an oil which solidified when triturated with cyclohexane. White solid, the title compound, in the amount of 4.0 g (75%) was collected, m.p. 80°-83° C.

Workup

  1. customThis compound was prepared
  2. customgave an oil which
  3. customtriturated with cyclohexane
  4. customWhite solid, the title compound, in the amount of 4.0 g (75%) was collected

Sources & evidence

ORD record
ord-825f4b0ba7684fc7bde3a17d439c4288
Source dataset
uspto-grants-1990_10
Patent number
US04960776

Reaction notes

Loading…