Sodium Hydroxide → HCID 66835207, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:12]=[C:11]2[C:6]([CH2:7][CH:8]([C:16]3[CH:21]=[CH:20][N:19]=[CH:18][C:17]=3[O:22]COC)[C:9](=[O:15])[C:10]2([CH3:14])[CH3:13])=[CH:5][CH:4]=1.O1CCOCC1.Cl.[OH-].[Na+]>>[OH:22][C:17]1[CH:18]=[N:19][CH:20]=[CH:21][C:16]=1[CH:8]1[CH2:7][C:6]2[C:11](=[CH:12][C:3]([O:2][CH3:1])=[CH:4][CH:5]=2)[C:10]([CH3:13])([CH3:14])[C:9]1=[O:15]Participants
4
Procedure
Mixture of 7-methoxy-3-(3-methoxymethoxy-pyridin-4-yl)-1,1-dimethyl-3,4-dihydro-1H-naphthalen-2-one (Compound GT15-8, 430 mg) and 4 N hydrochloric acid dioxane solution (5 ml) was heated and stirred at room temperature for 1.5 hrs. The reaction mixture was neutralized with 2 N aqueous solution of sodium hydroxide. The resulting mixture was extracted with the mixture of DCM and MeOH (DCM:MeOH=9:1). The residues obtained after concentration under reduced pressure were purified by silica gel column (DCM/MeOH) to obtain the title compound (280 mg, 75%).
Workup
- temperaturewas heated
- extractionThe resulting mixture was extracted with the mixture of DCM and MeOH (DCM:MeOH=9:1)
- customThe residues obtained
- concentrationafter concentration under reduced pressure
- customwere purified by silica gel column (DCM/MeOH)
Sources & evidence
- ORD record
- ord-2c1aaac69c564234950d59aa1dd606cf
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09126931B2
Reaction notes
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