Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 57681120 | HCID 57681120 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 16748464 | HCID 16748464 | — |
Reaction Steps
To a suspension of 4-[6-(4-trifluoromethyl-cyclohex-1-enyl)-pyrimidin-4-yloxy]-benzothiazol-2-ylamine, Example 1(e), (85 mg, 0.22 mmol) in toluene was added acetic anhydride (82 μL, 0.86 mmol). The mixture was heated at 90° C. with stirring for 1 h. The reaction mixture was allowed to cool to room temperature and evaporated in vacuo to give the title compound as a white solid. MS (ESI, pos. ion.) m/z: 435 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08227469B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-4ad1c82cfa0e41f7b5fe57b2d933cf9c |
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| Source note | uspto-grants-2012_07 |
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