1-Diethylamino ethyl-2-phenyl-3-keto piperazine → 1-(4'-Chloro benzyl)-3-phenyl-4-diethylamino ethyl piperazine

HRID 596858Notes

Reaction equation

HRID 596858 reaction equation
[Cl:1][C:2]1[CH:28]=[CH:27][C:5]([CH2:6][N:7]2[CH2:12][CH2:11][N:10]([CH2:13][CH2:14][N:15]([CH2:18][CH3:19])[CH2:16][CH3:17])[CH:9]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[C:8]2=O)=[CH:4][CH:3]=1.C(N(CC)C(N1CCNC(=O)C1C1C=CC=CC=1)C)C>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:6][N:7]2[CH2:12][CH2:11][N:10]([CH2:13][CH2:14][N:15]([CH2:18][CH3:19])[CH2:16][CH3:17])[CH:9]([C:20]3[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=3)[CH2:8]2)=[CH:27][CH:28]=1

Participants

3

Reactant 2

HCID 214485351-Diethylamino ethyl-2-phenyl-3-keto piperazineHCID 214485431-(4'-Chloro benzyl)-2-keto-3-phenyl-4-diethylamino ethyl piperazine2×

Product 1

HCID 214485731-(4'-Chloro benzyl)-3-phenyl-4-diethylamino ethyl piperazine

Procedure

1-(4'-Chloro benzyl)-2-keto-3-phenyl-4-diethylamino ethyl piperazine prepared according to Example 10, is reduced by following the procedure described hereinabove in Example 8 (a) whereby, in place of 1-diethylamino ethyl-3-keto-2-phenyl piperazine, the equimolecular amount of said 1-(4'-Chloro benzyl)-2-keto-3-phenyl-4-diethylamino ethyl piperazine is used. The resulting 3-phenyl piperazine compound is obtained in the form of a light yellow oil boiling at 180° C./0.01 mm. Hg.

Sources & evidence

ORD record
ord-232a63f539974043ace7942f04d506d7
Source dataset
uspto-grants-1977_03
Patent number
US04012389

Reaction notes

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