Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | HCID 10321598 | HCID 10321598 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 21865120 | HCID 21865120 | — |
Reaction Steps
To 2-bromo-4-[6-(4-trifluoromethyl-phenyl)-pyrimidin-4-yloxy]-benzothiazole, (Example 86), (90 mg, 0.2 mmol) dissolved in dioxane (1 mL) was added ethanolamine (0.06 mL, 1 mmol, Aldrich). The reaction mixture was heated in microwave synthesizer at 200° C. for 10 min, allowed to cool to room temperature and evaporated in vacuum. Purification of the residue by silica gel chromatography (1:1 of EtOAc/hexanes) provided the title compound as a white solid. MS (ESI, pos. ion) m/z: 433 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07144888B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-7d1c6708e81648bfb001c00fa2bcea2b |
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| Source note | uspto-grants-2006_12 |
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