Sodium Hydroxide → HCID 57471286, compound
Reaction equation
[CH2:1]([CH:8]1[C:17]2[C:12](=[CH:13][CH:14]=[C:15]([O:18][CH2:19][CH2:20][NH:21][S:22]([CH2:25][CH:26]3[CH2:28][CH2:27]3)(=[O:24])=[O:23])[CH:16]=2)[CH2:11][CH2:10][CH:9]1[NH:29][C:30](=O)OCC)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].[H-].[H-].[H-].[Li+].[Al+3].[OH-].[Na+].CC(O)C.[ClH:47]>C1COCC1.C(Cl)Cl>[ClH:47].[CH2:1]([CH:8]1[C:17]2[CH:16]=[C:15]([O:18][CH2:19][CH2:20][NH:21][S:22]([CH2:25][CH:26]3[CH2:28][CH2:27]3)(=[O:24])=[O:23])[CH:14]=[CH:13][C:12]=2[CH2:11][CH2:10][CH:9]1[NH:29][CH3:30])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
7
Procedure
The synthesis was performed starting from ethyl 1-benzyl-7-(2-(cyclopropylmethylsulfonamido)ethoxy)-1,2,3,4-tetrahydronaphthalen-2-ylcarbamate (synthesized in analogy to example 3), which was dissolved in THF (50 ml), after which LiAlH4 was added at room temperature and the mixture was stirred for 8 h under reflux. Addition of 2N aqueous NaOH, extraction with CH2Cl2, washing of the organic layers with saturated NaHCO3 solution and saturated NaCl solution and evaporation of the solvent gave a residue that was treated with iPrOH/HCl after which the product precipitated. After filtration a white salt (287 mg, 58%) were obtained.
Workup
- temperatureunder reflux
- washwashing of the organic layers with saturated NaHCO3 solution and saturated NaCl solution and evaporation of the solvent
- customgave a residue that
- customprecipitated
- filtrationAfter filtration a white salt (287 mg, 58%)
- customwere obtained
Sources & evidence
- ORD record
- ord-47d65b19476a41748b1a9bb2ba0ee131
- Source dataset
- uspto-grants-2015_08
- Patent number
- US09096619B2
Reaction notes
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