HCID 54345717, compound → HCID 54051398, compound

HRID 582023Notes

Reaction equation

HRID 582023 reaction equation
C([NH:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]2[CH:16]=[C:15]([C:17]3[CH:22]=[CH:21][C:20]([CH3:23])=[CH:19][CH:18]=3)[CH:14]=[C:13]([C:24]3[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=3)[N:12]=2)=[CH:7][CH:6]=1)(=O)C>N1C=CC=CC=1>[NH2:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]2[CH:16]=[C:15]([C:17]3[CH:22]=[CH:21][C:20]([CH3:23])=[CH:19][CH:18]=3)[CH:14]=[C:13]([C:24]3[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=3)[N:12]=2)=[CH:7][CH:6]=1

Participants

3

Reactant 1

HCID 54345717HCID 54345717, compound

Product 1

HCID 54051398HCID 54051398, compound

Reagents, catalysts & solvents 1

HCID 1049PyridineSolvent

Procedure

The following compound was obtained substantially in the same manner as above, using a corresponding pyridine derivative having an acetamide group in place of 2-(4-acetamidophenyl)-4-(4-methylphenyl)-6-phenylpyridine.

Workup

  1. customThe following compound was obtained substantially in the same manner as above,

Sources & evidence

ORD record
ord-c32cf593a8594122b39d5a14db441d5d
Source dataset
uspto-grants-1999_07
Patent number
US05922743

Reaction notes

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