Sodium Hydroxide → HCID 57467286, compound
Reaction equation
[CH:1]1([CH2:4][S:5]([NH:8][CH2:9][CH2:10][O:11][C:12]2[CH:21]=[C:20]3[C:15]([CH2:16][CH2:17][CH:18]([NH:30][C:31](=O)OCC)[CH:19]3[CH2:22][C:23]3[CH:28]=[CH:27][C:26]([F:29])=[CH:25][CH:24]=3)=[CH:14][CH:13]=2)(=[O:7])=[O:6])[CH2:3][CH2:2]1.[H-].[H-].[H-].[H-].[Li+].[Al+3].[OH-].[Na+].CC(O)C.Cl>C1COCC1.C(Cl)Cl>[CH:1]1([CH2:4][S:5]([NH:8][CH2:9][CH2:10][O:11][C:12]2[CH:13]=[CH:14][C:15]3[CH2:16][CH2:17][CH:18]([NH:30][CH3:31])[CH:19]([CH2:22][C:23]4[CH:24]=[CH:25][C:26]([F:29])=[CH:27][CH:28]=4)[C:20]=3[CH:21]=2)(=[O:6])=[O:7])[CH2:3][CH2:2]1Participants
7
Procedure
The synthesis was performed starting from ethyl 7-(2-(cyclopropylmethylsulfonamido)ethoxy)-1-(4-fluorobenzyl)-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 (89 mg, 76%) was 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 (89 mg, 76%)
- customwas obtained
Sources & evidence
- ORD record
- ord-1f3fa4b77ccd4cef9b7af9d29004510c
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09067871B2
Reaction notes
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