Hydrochloric Acid → HCID 71001800, compound
Reaction equation
Cl.[NH2:2][C:3]1[N:4]([CH2:26][CH3:27])[C:5]2[C:10]([C:11](=[O:24])[C:12]=1[C:13]([NH:15][CH2:16][CH:17](OCC)OCC)=[NH:14])=[CH:9][CH:8]=[C:7]([I:25])[CH:6]=2.[OH-].[Na+].[NH4+].[OH-]>O>[NH2:2][C:3]1[N:4]([CH2:26][CH3:27])[C:5]2[C:10]([C:11](=[O:24])[C:12]=1[C:13]1[NH:14][CH:17]=[CH:16][N:15]=1)=[CH:9][CH:8]=[C:7]([I:25])[CH:6]=2Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
0.37 ml of a 12N HCl solution were added at 0° C. to a suspension of 0.13 .g (0.28 mmol) of 2-amino-N-(2,2-diethoxy-ethyl)-1-ethyl-7-iodo-4-oxo-1,4-dihydro-quinoline-3-carboxamidine. The reaction mixture was stirred at room temperature during 16 hours. The reaction mixture was than diluted with 0.55 ml of water, basified with 0.32 ml of 1N NaOH solution, and 0.134 ml of an NH4OH solution. The mixture was then filtered and the resulting solid was washed with water, acetonitrile and pentane to give 0.08 g (0.21 mmol) of a brown solid.
Workup
- filtrationThe mixture was then filtered
- washthe resulting solid was washed with water, acetonitrile and pentane
Sources & evidence
- ORD record
- ord-2f16a52be11b4e5ea5346667ab4ff3b3
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09126972B2
Reaction notes
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