Pyridine, 3-(4-aminobutyl)- → HCID 13912797, compound
Reaction equation
[C:1]([C:4]1[CH:22]=[CH:21][C:7]([O:8][CH2:9][CH2:10][O:11][C:12]2[CH:13]=[C:14]([CH:18]=[CH:19][CH:20]=2)[C:15](O)=[O:16])=[C:6]([CH2:23][CH2:24][CH3:25])[C:5]=1[OH:26])(=[O:3])[CH3:2].[N:27]1[CH:32]=[CH:31][CH:30]=[C:29]([CH2:33][CH2:34][CH2:35][CH2:36][NH2:37])[CH:28]=1>>[C:1]([C:4]1[CH:22]=[CH:21][C:7]([O:8][CH2:9][CH2:10][O:11][C:12]2[CH:13]=[C:14]([CH:18]=[CH:19][CH:20]=2)[C:15]([NH:37][CH2:36][CH2:35][CH2:34][CH2:33][C:29]2[CH:28]=[N:27][CH:32]=[CH:31][CH:30]=2)=[O:16])=[C:6]([CH2:23][CH2:24][CH3:25])[C:5]=1[OH:26])(=[O:3])[CH3:2]Participants
3
Procedure
The reaction of 1.06 g of 3-[2-(4-acetyl-3hydroxy-2propylphenoxy)ethoxy]benzoic acid with 0.49 g of 3-pyridine butanamine according to Example 40 gave 1.20 g, mp 90°, (83% yield) of 3-[2-(4-Acetyl-3-hydroxy-2-propylphenoxy)ethoxy]-N-[4-(3-pyridinyl)butyl]benzamide, the title compound.
Sources & evidence
- ORD record
- ord-c681ee03fece43dda6d1ba66b50c6b29
- Source dataset
- uspto-grants-1987_06
- Patent number
- US04672066
Reaction notes
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