HCID 66701425, compound → HCID 66701320, compound
Reaction equation
[CH2:1]([C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:10]=[N:11][CH:12]=[C:13]([O:15][CH3:16])[CH:14]=2)=[CH:5][CH:4]=1)[CH3:2]>C(O)(=O)C>[CH2:1]([C:3]1[CH:4]=[CH:5][C:6]([CH:9]2[CH2:14][CH:13]([O:15][CH3:16])[CH2:12][NH:11][CH2:10]2)=[CH:7][CH:8]=1)[CH3:2]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 1.0 g (4.7 mmol) of 3-(4-ethylphenyl)-5-methoxypyridine in 120 ml of acetic acid was reacted according to General Method 5A. The solution was concentrated under reduced pressure. The crude product was purified by flash chromatography (silica gel, dichloromethane/methanol gradient). Yield: 880 mg (86% of theory)
Workup
- concentrationThe solution was concentrated under reduced pressure
- customThe crude product was purified by flash chromatography (silica gel, dichloromethane/methanol gradient)
Sources & evidence
- ORD record
- ord-64950271b4e84d9f99ebabaea811eaa9
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08987248B2
Reaction notes
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