Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 66575833 | HCID 66575833 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 86709611 | HCID 86709611 | 1,200% |
Reaction Steps
(4-(3,4-dichlorophenyl)piperazine-1-yl)(5-methyl-3-(2-(trifluoromethoxy)phenyl)isoxazol-4-yl)methanone (100 mg, 0.20 mmol) was dissolved in acetone (10 mL), cooled to 0° C. and slowly added with hydrochloric ethanol (10%, 73 mg, 0.20 mmol). The resultant product was stirred at room temperature for 8 hours, filtered, and dried so as to provide a white solid required compound (84 mg, 1.20 mmol, 78%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09132126B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-beccec944c33481e879e6afd09c6b7c2 |
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| Source note | uspto-grants-2015_09 |
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