HCID 25121543, compound → HCID 25121896, compound

HRID 1694770Notes

Reaction equation

HRID 1694770 reaction equation
[ClH:1].Cl.N1(CCOC2C=CC(N(C3C=CC(OCCN4CCCCC4)=CC=3)C(=O)C3C=CC([F:26])=CC=3)=CC=2)CCCCC1.Cl.Cl.N1(CCOC2C=CC(N(C3C=CC(OCCN4CCCCC4)=CC=3)C(=O)C3C=CC=CC=3)=CC=2)CCCCC1.Cl.Cl.[N:86]1([CH2:92][CH2:93][O:94][C:95]2[CH:100]=[CH:99][C:98]([N:101]([C:119]3[CH:124]=[CH:123][CH:122]=[CH:121][CH:120]=3)[C:102](=[O:118])[C:103]3[CH:108]=[CH:107][C:106]([O:109][CH2:110][CH2:111][N:112]4[CH2:117][CH2:116][CH2:115][CH2:114][CH2:113]4)=[CH:105][CH:104]=3)=[CH:97][CH:96]=2)[CH2:91][CH2:90][CH2:89][CH2:88][CH2:87]1>>[ClH:1].[ClH:1].[F:26][C:122]1[CH:121]=[CH:120][C:119]([N:101]([C:98]2[CH:97]=[CH:96][C:95]([O:94][CH2:93][CH2:92][N:86]3[CH2:91][CH2:90][CH2:89][CH2:88][CH2:87]3)=[CH:100][CH:99]=2)[C:102](=[O:118])[C:103]2[CH:108]=[CH:107][C:106]([O:109][CH2:110][CH2:111][N:112]3[CH2:113][CH2:114][CH2:115][CH2:116][CH2:117]3)=[CH:105][CH:104]=2)=[CH:124][CH:123]=1

Participants

4

Reactant 3

HCID 25121543HCID 25121543, compoundHCID 25121544HCID 25121544, compoundHCID 25121546HCID 25121546, compound

Product 1

HCID 25121896HCID 25121896, compound

Procedure

N,N-Bis[4-(2-piperidin-1-ylethoxy)-phenyl]-4-fluoro-benzamide dihydrochloride (4s); N,N-Bis[4-(2-piperidin-1-ylethoxy)-phenyl]-benzamide dihydrochloride (4t); and N-[4-(2-piperidin-1-ylethoxy)-phenyl]-N-phenyl-[4-(2-piperidin-1-ylethoxy)]-benzamide dihydrochloride (4u).

Sources & evidence

ORD record
ord-415fd1a98e9948c1943e4c6416565b72
Source dataset
uspto-grants-2012_04
Patent number
US08158828B2

Reaction notes

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