Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(Methanesulfonyl)pyrimidine | HCID 13289225 | — |
| Reactant | HCID 118161922 | HCID 118161922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 118161935 | HCID 118161935 | 63.2% |
Reaction Steps
2-((5-(4-(trifluoromethoxy)phenyl)benzo[d]isoxazol-3-yl)oxy)ethanamine hydrochloride (57 mg, 0.152 mmol) and 2-(methylsulfonyl)pyrimidine (96 mg, 0.608 mmol) were dissolved in 2 mL ethanol in a microwave vial. Triethylamine (0.1 mL) was added and the mixture was heated at 120° C. for one hour in the microwave. All volatiles were removed under vacuum and the residue was purified on 12 g silica gel with 0-100% ethyl acetate in hexane to give the title compound (40 mg, 0.096 mmol). MS: 417 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09416115B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-8ac4a82e4d5e4de2b62a774f571f0c44 |
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| Source note | uspto-grants-2016_08 |
|---|