2,6-Dichloroquinoline-3-carboxylic acid → HCID 45255587, compound
Reaction equation
Cl[C:2]1[C:11]([C:12]([OH:14])=[O:13])=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([Cl:15])[CH:8]=2)[N:3]=1.[NH2:16][CH:17]([CH2:29][OH:30])[C:18]([NH:20][C:21]1[CH:26]=[CH:25][CH:24]=[C:23]([O:27][CH3:28])[CH:22]=1)=[O:19]>>[Cl:15][C:7]1[CH:8]=[C:9]2[C:4](=[CH:5][CH:6]=1)[N:3]=[C:2]([NH:16][CH:17]([C:18](=[O:19])[NH:20][C:21]1[CH:26]=[CH:25][CH:24]=[C:23]([O:27][CH3:28])[CH:22]=1)[CH2:29][OH:30])[C:11]([C:12]([OH:14])=[O:13])=[CH:10]2Participants
3
Procedure
In close analogy to the procedure described in Example 43, 2,6-dichloroquinoline-3-carboxylic acid is reacted with 2-amino-3-hydroxy-N-(3-methoxy-phenyl)-propionamide to provide the title compound in good yield. LCMS m/z 416 (M+1).
Sources & evidence
- ORD record
- ord-f2c6fbc3908946a0940a65c3570e8ea5
- Source dataset
- uspto-grants-2012_10
- Patent number
- US08288549B2
Reaction notes
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