5-Chloro-2-picolinic acid → HCID 67147784, compound
Reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH2:12][CH2:11][CH:10]([N:13]([CH3:15])[CH3:14])[CH2:9]2)=[CH:4][CH:3]=1.[Cl:16][C:17]1[CH:18]=[CH:19][C:20]([C:23](O)=[O:24])=[N:21][CH:22]=1>>[CH3:14][N:13]([CH3:15])[CH:10]1[CH2:11][CH2:12][N:8]([C:5]2[CH:6]=[CH:7][C:2]([NH:1][C:23]([C:20]3[CH:19]=[CH:18][C:17]([Cl:16])=[CH:22][N:21]=3)=[O:24])=[CH:3][CH:4]=2)[CH2:9]1Participants
3
Procedure
[1-(4-Aminophenyl)pyrrolidin-3-yl]dimethylamine was reacted with 5-chloropyridine-2-carboxylic acid by method E. This resulted in the product with the molecular weight of 344.85 (C18H21CIN4O); MS (ESI): 345 (M+H+).
Workup
- customThis resulted in the product with the molecular weight of 344.85 (C18H21CIN4O)
Sources & evidence
- ORD record
- ord-f9d138fd658a46beafee4d29a4bf1632
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07968550B2
Reaction notes
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