Hydrochloric Acid → HCID 10226339, compound
Reaction equation
[CH2:1]([N:3]([CH2:29][CH3:30])[CH2:4][CH2:5][C:6]1[C:14]2[C:9](=[CH:10][CH:11]=[C:12]([NH:15][S:16]([C:19]3[C:28]4[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=4)[CH:22]=[CH:21][CH:20]=3)(=[O:18])=[O:17])[CH:13]=2)[NH:8][CH:7]=1)[CH3:2].[ClH:31]>C(O)C>[ClH:31].[CH2:29]([N:3]([CH2:1][CH3:2])[CH2:4][CH2:5][C:6]1[C:14]2[C:9](=[CH:10][CH:11]=[C:12]([NH:15][S:16]([C:19]3[C:28]4[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=4)[CH:22]=[CH:21][CH:20]=3)(=[O:17])=[O:18])[CH:13]=2)[NH:8][CH:7]=1)[CH3:30]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
1.05 g (2.5 mMol) of N-[3-(2-diethylaminoethyl)-1H-indol-5-yl]naphthalene-1-sulphonamide (example 2) are dissolved in 10 ml of ethanol and 0.6 ml are added of a 4.2 N solution of hydrochloric acid in ethanol. It is allowed to crystallise at ambient temperature. N-[3-(2-diethylaminoethyl)-1H-indol-5-yl]naphthalene-1-sulphonamide hydrochloride is obtained as a solid with m.p.=255-257° C.
Workup
- customto crystallise at ambient temperature
Sources & evidence
- ORD record
- ord-bbe38b21f1884409ba46563e39eeffe4
- Source dataset
- uspto-grants-2009_03
- Patent number
- US07498328B2
Reaction notes
Loading…