Sodium Bicarbonate → HCID 9977407, compound
Reaction equation
[Cl:1][C:2]1[CH:34]=[CH:33][C:5]2[S:6][C:7]3[CH:32]=[CH:31][CH:30]=[CH:29][C:8]=3[C:9]3[N:10](COCC[Si](C)(C)C)[C:11]([CH2:14][O:15][CH2:16][CH2:17][N:18]([CH3:20])[CH3:19])=[N:12][C:13]=3[C:4]=2[CH:3]=1.C(=O)([O-])O.[Na+]>CO.Cl.O>[Cl:1][C:2]1[CH:34]=[CH:33][C:5]2[S:6][C:7]3[CH:32]=[CH:31][CH:30]=[CH:29][C:8]=3[C:9]3[NH:10][C:11]([CH2:14][O:15][CH2:16][CH2:17][N:18]([CH3:20])[CH3:19])=[N:12][C:13]=3[C:4]=2[CH:3]=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 3
Procedure
To a solution of {2-[5-chloro-1-(2-trimethylsilyl-ethoxymethyl)-1H-8-thia-1,3-diaza-dibenzo[e,h]azulene-2-ylmethoxy]-ethyl}-dimethyl-amine (0.21 mmole) in methanol (6.0 ml), 0.5 M hydrochloric acid in methanol (2.0 ml) was slowly added. The reaction mixture was heated under reflux for 3 hours, then it was cooled to room temperature, neutralized with a saturated aqueous solution of sodium hydrogencarbonate, diluted with water and extracted with dichloromethane. The organic extract was washed with an aqueous sodium chloride solution, dried over anhydrous Na2SO4 and evaporated under reduced pressure. After purification by chromatography on a silica gel column, [2-(5-chloro-1H-8-thia-1,3-diaza-dibenzo[e,h]azulene-2-ylmethoxy)-ethyl]-dimethyl-amine in the form of an oily product was obtained;
Workup
- temperatureThe reaction mixture was heated
- temperatureunder reflux for 3 hours
- extractionextracted with dichloromethane
- extractionThe organic extract
- washwas washed with an aqueous sodium chloride solution
- dry with materialdried over anhydrous Na2SO4
- customevaporated under reduced pressure
- customAfter purification by chromatography on a silica gel column, [2-(5-chloro-1H-8-thia-1,3-diaza-dibenzo[e,h]azulene-2-ylmethoxy)-ethyl]-dimethyl-amine in the form of an oily product
- customwas obtained
Sources & evidence
- ORD record
- ord-3c3fe7b7649142ac92af4b692aea2a73
- Source dataset
- uspto-grants-2007_01
- Patent number
- US07166583B2
Reaction notes
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