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3-Methyl-5-(trifluoromethyl)benzoic acid → N-[(3R,4R)-1-[(1-acetylpiperidin-4-yl)carbonyl]-3-(3,4-dichlorophenyl)piperidin-4-yl]-N,3-dimethyl-5-(trifluoromethyl)benzamide

HRID 1260952
Notes
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Reaction equation

HRID 1260952 reaction equation
[C:1]([N:4]1[CH2:9][CH2:8][CH:7]([C:10]([N:12]2[CH2:17][CH2:16][C@@H:15]([NH:18][CH3:19])[C@H:14]([C:20]3[CH:25]=[CH:24][C:23]([Cl:26])=[C:22]([Cl:27])[CH:21]=3)[CH2:13]2)=[O:11])[CH2:6][CH2:5]1)(=[O:3])[CH3:2].[CH3:28][C:29]1[CH:30]=[C:31]([CH:35]=[C:36]([C:38]([F:41])([F:40])[F:39])[CH:37]=1)[C:32]([OH:34])=O>>[C:1]([N:4]1[CH2:5][CH2:6][CH:7]([C:10]([N:12]2[CH2:17][CH2:16][C@@H:15]([N:18]([CH3:19])[C:32](=[O:34])[C:31]3[CH:35]=[C:36]([C:38]([F:41])([F:40])[F:39])[CH:37]=[C:29]([CH3:28])[CH:30]=3)[C@H:14]([C:20]3[CH:25]=[CH:24][C:23]([Cl:26])=[C:22]([Cl:27])[CH:21]=3)[CH2:13]2)=[O:11])[CH2:8][CH2:9]1)(=[O:3])[CH3:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 27755883-Methyl-5-(trifluoromethyl)benzoic acidHCID 57741761(3R*,4R*)-1-[(1-acetylpiperidin-4-yl)carbonyl]-3-(3,4-dichlorophenyl)-N-methylpiperidin-4-amine

Product 1

HCID 68929046N-[(3R,4R)-1-[(1-acetylpiperidin-4-yl)carbonyl]-3-(3,4-dichlorophenyl)piperidin-4-yl]-N,3-dimethyl-5-(trifluoromethyl)benzamide

Procedure

Using the compound obtained in Example 78 and 3-methyl-5-trifluoromethylbenzoic acid, and by the reaction and purification in the same manner as in Example 3, the title compound was obtained.

Workup

  • customby the reaction and purification in the same manner as in Example 3
  • Sources & evidence

    ORD record
    ord-ae1f4930e217458ebbabb35181b82536
    Source dataset
    uspto-grants-2013_06
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US08470816B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes