Triethylamine → 2-Hydroxy-2-(4-methanesulphonamidophenyl)-N-methyl-N-[2-(5-phenyl-2H-pyridazin-3-on-2-yl)ethyl] ethylamine
Reaction equation
[C:1]1([C:7]2[CH:12]=[N:11][N:10]([CH2:13][CH2:14]Br)[C:9](=[O:16])[CH:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH:17][CH:18]([C:22]1[CH:27]=[CH:26][C:25]([NH:28][S:29]([CH3:32])(=[O:31])=[O:30])=[CH:24][CH:23]=1)[CH2:19][NH:20][CH3:21].C(N(CC)CC)C>C(O)C>[OH:17][CH:18]([C:22]1[CH:23]=[CH:24][C:25]([NH:28][S:29]([CH3:32])(=[O:31])=[O:30])=[CH:26][CH:27]=1)[CH2:19][N:20]([CH3:21])[CH2:14][CH2:13][N:10]1[C:9](=[O:16])[CH:8]=[C:7]([C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)[CH:12]=[N:11]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
2-[5-Phenyl-2H-pyridazin-3-on-2-yl]ethyl bromide (0.28 g), 2-hydroxy-N-methyl-2-(4-methanesulphonamidophenyl)ethylamine (0.24 g) and triethylamine (0.22 g) were refluxed in ethanol (30 ml) for 4 hours. The solvent was removed and the residue taken up in methylene chloride, washed with water, evaporated and the residue chromatographed on silica [Merck `Kieselgel 60` (Trade Mark)], eluting with ethyl acetate. Collection and evaporation of appropriate fractions gave the title compound as a solid which was recrystallised from diisopropyl ether, yield 0.1 g, m.p. 108°.
Workup
- customThe solvent was removed
- washwashed with water
- customevaporated
- customthe residue chromatographed on silica [Merck `Kieselgel 60` (Trade Mark)],
- washeluting with ethyl acetate
- customCollection and evaporation of appropriate fractions
Sources & evidence
- ORD record
- ord-429f3570171d4035991a0250c77d728d
- Source dataset
- uspto-grants-1992_05
- Patent number
- US05114952
Reaction notes
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