Hydrochloric Acid → HCID 18770465, compound

HRID 1279476Notes

Reaction equation

HRID 1279476 reaction equation
[ClH:1].[CH3:2][O:3][C:4]1[CH:5]=[C:6]([C:14]2[CH:61]=[CH:60][C:17]([C:18]([N:20]3[CH2:25][CH2:24][CH:23]([CH2:26][N:27]4[CH2:32][CH2:31][N:30]([CH2:33][CH:34]5[CH2:39][CH2:38][N:37]([C:40](=[O:59])[C:41]6[CH:46]=[CH:45][C:44]([C:47]7[CH:52]=[C:51]([O:53][CH3:54])[C:50]([O:55][CH3:56])=[C:49]([O:57][CH3:58])[CH:48]=7)=[CH:43][CH:42]=6)[CH2:36][CH2:35]5)[CH2:29][CH2:28]4)[CH2:22][CH2:21]3)=[O:19])=[CH:16][CH:15]=2)[CH:7]=[C:8]([O:12][CH3:13])[C:9]=1[O:10][CH3:11]>C(O)C>[ClH:1].[ClH:1].[CH3:58][O:57][C:49]1[CH:48]=[C:47]([C:44]2[CH:43]=[CH:42][C:41]([C:40]([N:37]3[CH2:36][CH2:35][CH:34]([CH2:33][N:30]4[CH2:29][CH2:28][N:27]([CH2:26][CH:23]5[CH2:22][CH2:21][N:20]([C:18](=[O:19])[C:17]6[CH:16]=[CH:15][C:14]([C:6]7[CH:5]=[C:4]([O:3][CH3:2])[C:9]([O:10][CH3:11])=[C:8]([O:12][CH3:13])[CH:7]=7)=[CH:61][CH:60]=6)[CH2:25][CH2:24]5)[CH2:32][CH2:31]4)[CH2:39][CH2:38]3)=[O:59])=[CH:46][CH:45]=2)[CH:52]=[C:51]([O:53][CH3:54])[C:50]=1[O:55][CH3:56]

Participants

4

Procedure

Concentrated hydrochloric acid (0.050 ml; 0.60 mmol) was added to a solution of 1,4-bis[[1-[4-(3,4,5-trimethoxyphenyl)benzoyl]-4-piperidinyl]methyl]piperazine (100 mg; 0.12 mmol) in ethanol (5 ml) and the reaction mixture was concentrated under reduced pressure. After a process of adding ethanol (10 ml) to the residue and concentrating the mixture under reduced pressure was performed twice, the resultant concentrated residue was recrystallized from methanol-diethyl ether to obtain the title compound as colorless needles.

Workup

  1. concentrationthe reaction mixture was concentrated under reduced pressure
  2. concentrationAfter a process of adding ethanol (10 ml) to the residue and concentrating the mixture under reduced pressure
  3. customthe resultant concentrated residue was recrystallized from methanol-diethyl ether

Sources & evidence

ORD record
ord-65d1b92d7a054633bccd43268eaf442b
Source dataset
uspto-grants-2002_09
Patent number
US06448242B1

Reaction notes

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