2-[N-Ethyl-N-(2-(phenethyl)benzyl)amino]pyridine-5-carboxylic acid → 4-[2-(Phenethyl)phenethyl]benzoic acid
Reaction equation
[CH2:1]([C:9]1[CH:26]=[CH:25][CH:24]=[CH:23][C:10]=1[CH2:11][CH2:12][C:13]1[CH:22]=[CH:21][C:16]([C:17]([O:19]C)=[O:18])=[CH:15][CH:14]=1)[CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.C(N(C1C=CC(C(O)=O)=CN=1)CC1C=CC=CC=1CCC1C=CC=CC=1)C>>[CH2:1]([C:9]1[CH:26]=[CH:25][CH:24]=[CH:23][C:10]=1[CH2:11][CH2:12][C:13]1[CH:14]=[CH:15][C:16]([C:17]([OH:19])=[O:18])=[CH:21][CH:22]=1)[CH2:2][C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=1Participants
3
Procedure
The title compound was prepared from methyl 4-[2-(phenethyl)phenethyl]benzoate using a similar method to that of Example 24 paragraph (A).
Sources & evidence
- ORD record
- ord-dc1d3dd9a28640e299ad753e574618ae
- Source dataset
- uspto-grants-1998_11
- Patent number
- US05834468
Reaction notes
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