Hydrochloric Acid → 1-[2-[3-(3,4-Dichloro-phenyl)-1-(3,4,5-trimethoxy-benzoyl)-pyrrolidin-3-yl]-ethyl]-4-phenyl-piperidine-4-carboxylic acid 4-methylpiperazine-amide hydrochloride

HRID 1683109Notes

Reaction equation

HRID 1683109 reaction equation
[CH3:1][N:2]1[CH2:7][CH2:6][N:5]([C:8]([NH2:10])=[O:9])[CH2:4][CH2:3]1.[Cl:11][C:12]1[CH:13]=[C:14]([C:19]2([CH2:38][CH2:39][N:40]3[CH2:45][CH2:44][C:43]([C:49]4[CH:54]=[CH:53][CH:52]=[CH:51][CH:50]=4)([C:46]([OH:48])=[O:47])[CH2:42][CH2:41]3)[CH2:23][CH2:22][N:21]([C:24](=[O:37])[C:25]3[CH:30]=[C:29]([O:31][CH3:32])[C:28]([O:33][CH3:34])=[C:27]([O:35][CH3:36])[CH:26]=3)[CH2:20]2)[CH:15]=[CH:16][C:17]=1[Cl:18].Cl>ClCCl>[ClH:11].[CH3:1][N:2]1[CH2:7][CH2:6][N:5]([C:8]([NH2:10])=[O:9])[CH2:4][CH2:3]1.[Cl:11][C:12]1[CH:13]=[C:14]([C:19]2([CH2:38][CH2:39][N:40]3[CH2:45][CH2:44][C:43]([C:49]4[CH:54]=[CH:53][CH:52]=[CH:51][CH:50]=4)([C:46]([OH:48])=[O:47])[CH2:42][CH2:41]3)[CH2:23][CH2:22][N:21]([C:24](=[O:37])[C:25]3[CH:30]=[C:29]([O:31][CH3:32])[C:28]([O:33][CH3:34])=[C:27]([O:35][CH3:36])[CH:26]=3)[CH2:20]2)[CH:15]=[CH:16][C:17]=1[Cl:18]

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 675594611-[2-[3-(3,4-Dichloro-phenyl)-1-(3,4,5-trimethoxy-benzoyl)-pyrrolidin-3-yl]-ethyl]-4-phenyl-piperidine-4-carboxylic acid 4-methylpiperazine-amide

Product 1

HCID 675622111-[2-[3-(3,4-Dichloro-phenyl)-1-(3,4,5-trimethoxy-benzoyl)-pyrrolidin-3-yl]-ethyl]-4-phenyl-piperidine-4-carboxylic acid 4-methylpiperazine-amide hydrochloride

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent2×

Procedure

Dissolve 1-[2-[3-(3,4-dichloro-phenyl)-1-(3,4,5-trimethoxy-benzoyl)-pyrrolidin-3-yl]-ethyl]-4-phenyl-piperidine-4-carboxylic acid 4-methylpiperazine-amide (1.96 g, 2.71 mmol) in dichloromethane (20 mL). This solution was combined with a saturated solution of hydrochloric acid in dichloromethane (20 mL) and the mixture was stirred for 1 hour. The reaction mixture was evaporated [in vacuo and hexane was added. This mixture was evaporated in vacuo and diethyl ether was added. The diethyl ether mixture was evaporated in vacuo to give a solid. The solid was dried in vacuo to give the title compound.

Workup

  1. customThe reaction mixture was evaporated [in vacuo and hexane
  2. additionwas added
  3. customThis mixture was evaporated in vacuo and diethyl ether
  4. additionwas added
  5. customThe diethyl ether mixture was evaporated in vacuo
  6. customto give a solid
  7. customThe solid was dried in vacuo

Sources & evidence

ORD record
ord-d99f778c58f042c88285e4283ca78e59
Source dataset
uspto-grants-1997_06
Patent number
US05635510

Reaction notes

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