Hydrochloric Acid → HCID 76071674, compound
Reaction equation
C(OC(=O)[NH:7][C:8]1[C:9]([C:13]2[CH:18]=[CH:17][C:16]([CH2:19][CH2:20][C:21]3[CH:26]=[CH:25][C:24]([S:27]([CH3:30])(=[O:29])=[O:28])=[CH:23][CH:22]=3)=[CH:15][CH:14]=2)=[N:10][O:11][CH:12]=1)(C)(C)C.Cl>O1CCOCC1>[CH3:30][S:27]([C:24]1[CH:23]=[CH:22][C:21]([CH2:20][CH2:19][C:16]2[CH:17]=[CH:18][C:13]([C:9]3[C:8]([NH2:7])=[CH:12][O:11][N:10]=3)=[CH:14][CH:15]=2)=[CH:26][CH:25]=1)(=[O:28])=[O:29]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
(3-{4-[2-(4-Methanesulfonyl-phenyl)-ethyl]-phenyl}-isoxazol-4-yl)-carbamic acid tert-butyl ester (88 mg, 0.2 mmol) was dissolved in dioxane (2 mL) and 4N HCl in dioxane (4 mL) was added dropwise. The reaction mixture was stirred at rt for 24.5 h and 3-{4-[2-(4-methanesulfonyl-phenyl)-ethyl]-phenyl}-isoxazol-4-ylamine hydrochloride (53 mg, 71%) was collected by filtration as a white solid. HRMS: 343.111 (M+1)
Workup
- filtration3-{4-[2-(4-methanesulfonyl-phenyl)-ethyl]-phenyl}-isoxazol-4-ylamine hydrochloride (53 mg, 71%) was collected by filtration as a white solid
Sources & evidence
- ORD record
- ord-238716cc6c0b45c99c0f5ce3c3e918c6
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09290465B2
Reaction notes
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