Hydrochloric Acid → HCID 17910543, compound
Reaction equation
[C:1]([C:4]1[CH:9]=[CH:8][C:7]([CH2:10][CH2:11][C:12]([N:14]2[C:23]3[C:18](=[CH:19][C:20]([N:24]([CH2:34][C:35]([O:37]CC)=[O:36])[S:25]([C:28]4[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=4)(=[O:27])=[O:26])=[CH:21][CH:22]=3)[CH2:17][CH2:16][CH2:15]2)=[O:13])=[CH:6][CH:5]=1)(=[NH:3])[NH2:2].[OH-].[Na+].Cl>C(O)C>[C:1]([C:4]1[CH:9]=[CH:8][C:7]([CH2:10][CH2:11][C:12]([N:14]2[C:23]3[C:18](=[CH:19][C:20]([N:24]([CH2:34][C:35]([OH:37])=[O:36])[S:25]([C:28]4[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=4)(=[O:26])=[O:27])=[CH:21][CH:22]=3)[CH2:17][CH2:16][CH2:15]2)=[O:13])=[CH:6][CH:5]=1)(=[NH:2])[NH2:3]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
370 mg of 1-[3-(4-amidino-phenyl)propionyl]-6-(N-ethoxycarbonylmethyl-phenylsulphonamido)-1,2,3,4-tetrahydro-quinoline are dissolved in 5 ml of ethanol and stirred overnight with 1.6 ml of 1N sodium hydroxide solution. Then the mixture is neutralised with hydrochloric acid, concentrated by evaporation and the residue is chromatographed with methanol over a silica gel column.
Workup
- concentrationconcentrated by evaporation
- customthe residue is chromatographed with methanol over a silica gel column
Sources & evidence
- ORD record
- ord-beeaafdc6ad54fd4b0dc957f60bce999
- Source dataset
- uspto-grants-2001_10
- Patent number
- US06300342B1
Reaction notes
Loading…