Hydrochloric Acid → HCID 76071680, compound
Reaction equation
C(OC(=O)[NH:7][C:8]1[C:9]([C:13]2[CH:18]=[CH:17][C:16]([O:19][CH2:20][C:21](=[O:28])[C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)=[CH:15][CH:14]=2)=[N:10][O:11][CH:12]=1)(C)(C)C.[ClH:30]>O1CCOCC1>[ClH:30].[NH2:7][C:8]1[C:9]([C:13]2[CH:14]=[CH:15][C:16]([O:19][CH2:20][C:21]([C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)=[O:28])=[CH:17][CH:18]=2)=[N:10][O:11][CH:12]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
{3-[4-(2-Oxo-2-phenyl-ethoxy)-phenyl]-isoxazol-4-yl}-carbamic acid tert-butyl ester (70 mg, 0.18 mmol) was dissolved in dioxane (1 mL) and treated with 4N HCl in dioxane (1 mL, 4 mmol). After stirring overnight the resulting white solid was removed by filtration and washed with hexanes to yield 2-[4-(4-Amino-isoxazol-3-yl)-phenoxy]-1-phenyl-ethanone hydrochloride as a white solid (34 mg, 64%). MH+=295.0
Workup
- customwas removed by filtration
- washwashed with hexanes
Sources & evidence
- ORD record
- ord-837c639176894bb58b4f9d5df8030a90
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09290465B2
Reaction notes
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