Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Fluoro-5-(trifluoromethyl)benzoyl Chloride | HCID 2734880 | — |
| Reactant | [2-(3-Amino-4-chloro-phenoxy)-[3,4']bipyridinyl-2'-yl]-methyl-amine | HCID 66970380 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 58588060 | HCID 58588060 | — |
Reaction Steps
In a sealed tube, [2-(3-Amino-4-chloro-phenoxy)-[3,4′]bipyridinyl-2′-yl]-methyl-amine (300 mg, 0.918 mmol) and 2-Fluoro-5-trifluoromethyl-benzoyl chloride (0.180 mL, 1.19 mmol) were dissolved in 2.0 mL chloroform. The solution was heated to 75° C. and stirred for 48 h. The reaction was then cooled to RT, quenched with triethylamine (0.128 mL, 0.918 mmol), and concentrated in vacuo to yield the title compound as a crude light yellow solid. MS m/z (M+H)+=517; Calc'd 516.87 for C25H17ClF4N4O2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07880000B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-1dfd803df74c471195a908cda5893621 |
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| Source note | uspto-grants-2011_02 |
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