Hydrochloric Acid → N-(6-aminoquinolin-5-yl)-2-(hexylthio)decanoic amide
Reaction equation
[NH:1]([C:5]1[C:6]([NH:15][C:16](=[O:33])[CH:17]([S:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])=[C:7]2[C:12](=[CH:13][CH:14]=1)[N:11]=[CH:10][CH:9]=[CH:8]2)C(C)=O.Cl>C(O)(C)C>[NH2:1][C:5]1[C:6]([NH:15][C:16](=[O:33])[CH:17]([S:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])=[C:7]2[C:12](=[CH:13][CH:14]=1)[N:11]=[CH:10][CH:9]=[CH:8]2Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
N-(6-Acetaminoquinolin-5-yl)-2-(hexylthio)decanoic amide, prepared as described in Example 151, was treated with aqueous hydrochloric acid and isopropanol to give the title compound. Mass spectrum m/e: 428.3 (M+-1).
Sources & evidence
- ORD record
- ord-362493da281c46db957f3a74944d0472
- Source dataset
- uspto-grants-1994_11
- Patent number
- US05362878
Reaction notes
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