Hydrochloric Acid → HCID 20150448, compound
Reaction equation
C[O:2][C:3]1[CH:12]=[CH:11][C:10]2[C:5](=[C:6]([CH3:23])[CH:7]=[C:8]([C:13]3[CH:18]=[CH:17][C:16]([C:19]([O:21][CH3:22])=[O:20])=[CH:15][CH:14]=3)[CH:9]=2)[N:4]=1.Cl>>[CH3:23][C:6]1[CH:7]=[C:8]([C:13]2[CH:18]=[CH:17][C:16]([C:19]([O:21][CH3:22])=[O:20])=[CH:15][CH:14]=2)[CH:9]=[C:10]2[C:5]=1[NH:4][C:3](=[O:2])[CH:12]=[CH:11]2Participants
3
Procedure
0.5H2O, m.p. 293°, was prepared similarly to Example 13(A) using 2-methoxy-8-methyl-6-(4-methoxycarbonylphenyl)quinoline and 5M HCl.
Workup
- custom0.5H2O, m.p. 293°, was prepared similarly to Example 13(A)
Sources & evidence
- ORD record
- ord-46d6cbe76ffc4092b09e0f2587552d59
- Source dataset
- uspto-grants-1988_03
- Patent number
- US04728654
Reaction notes
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