Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178512072 | HCID 178512072 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 87543951 | HCID 87543951 | — |
Reaction Steps
To a solution of (S)—N-(1-(4-(4-chlorophenoxy)phenyl)-5-(3-(trifluoromethyl)-phenyl)imidazolidin-2-ylidene)cyanamide [prepared from Example 203] (15.0 mg, 0.033 mmol) in 1,4-dioxane (0.5 mL) is treated with excess BrCN and K2CO3. The reaction mixture is heated at 100° C. for 2 h, cooled, then quenched with H2O (5 mL) and extracted with EtOAc (3×3 mL). The combined organics are evaporated en vacuo and purified by preparatory LC/MS followed by preparatory TLC to provide the title compound; HPLC-MS calculated for C24H15ClF3N5O (M+H+) 482.1, found 482.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08431607B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-0ac56ea7dfe441e990354a1e9a90c18e |
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| Source note | uspto-grants-2013_04 |
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