Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 59320927 | HCID 59320927 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59321125 | HCID 59321125 | — |
Reaction Steps
To a solution of 1-[3-(7-Hydrazinocarbonyl-imidazo[1,2-a]pyridin-3-yl)-phenyl]-3-(2,2,2-trifluoro-ethyl)-urea (120 mg, 0.30 mmol) and KOH (20 mg, 0.36 mmol) in EtOH (4 ml) was added carbon disulfide (241, 0.36 mmol). The reaction mixture was heated at 65° C. for 3 h. Methyl iodide (200, excess) was added and the reaction mixture heated at 65° C. for 1 h. The mixture was then cooled, placed in an ice bath upon which a precipitate was formed. The solid was filtered off, washed with EtOAc and Et2O, then dried to afford the title compound (89 mg). MS: [M+H]+=449.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08895745B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-3bf921fc6b394a9c8e5b1345c8344ed9 |
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| Source note | uspto-grants-2014_11 |
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