Ethanolamine → HCID 136353746, compound
Reaction equation
[CH2:1]([NH2:4])[CH2:2][OH:3].[CH3:5][C:6]1[NH:10][C:9](=[O:11])[N:8]([C:12]2[CH:17]=[CH:16][C:15]([S:18][C:19]3[CH:20]=[C:21]([C:25]4([C:31](OCC)=[O:32])[CH2:30][CH2:29][O:28][CH2:27][CH2:26]4)[CH:22]=[CH:23][CH:24]=3)=[CH:14][CH:13]=2)[N:7]=1>C(O)C>[OH:3][CH2:2][CH2:1][NH:4][C:31]([C:25]1([C:21]2[CH:22]=[CH:23][CH:24]=[C:19]([S:18][C:15]3[CH:16]=[CH:17][C:12]([N:8]4[C:9](=[O:11])[NH:10][C:6]([CH3:5])=[N:7]4)=[CH:13][CH:14]=3)[CH:20]=2)[CH2:30][CH2:29][O:28][CH2:27][CH2:26]1)=[O:32]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2-Ethanolamine (6.0 mmol) is added to a solution of ethyl 4-(3-{[4-(3-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl)phenyl]thio}phenyl)tetrahydro-2H-pyran-4-carboxylate (1.0 mmol) (example 19) in ethanol and the mixture are refluxed. All the volatiles are removed under reduced pressure and the residue is purified by column chromatography over silica gel to afford the title compound.
Workup
- temperaturethe mixture are refluxed
- customAll the volatiles are removed under reduced pressure
- customthe residue is purified by column chromatography over silica gel
Sources & evidence
- ORD record
- ord-3bf0342b95794bde85ca816b29ebf1e7
- Source dataset
- uspto-grants-2010_03
- Patent number
- US07674811B2
Reaction notes
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