Oxalyl chloride → N-(7-phenyl-heptyl)-3-pyridin-3-yl-acrylamide
Reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH:7]=[CH:8][C:9]([OH:11])=O)[CH:2]=1.C(Cl)(=O)C(Cl)=O.[C:18]1([CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][NH2:31])[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>>[C:18]1([CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][NH:31][C:9](=[O:11])[CH:8]=[CH:7][C:3]2[CH:2]=[N:1][CH:6]=[CH:5][CH:4]=2)[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1Participants
4
Procedure
Batch size: 5.1 g (33.9 mmol) 3-(3-pyridyl)-acrylic acid, 6.6 ml (76.4 mmol) oxalyl chloride and 5.9 g (30.8 mmol) 7-phenyl-heptylamine.
Sources & evidence
- ORD record
- ord-f8ae539a005c403ba9680eda9b021e31
- Source dataset
- uspto-grants-2008_01
- Patent number
- US07320993B1
Reaction notes
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