Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | HCID 58154781 | HCID 58154781 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 44552710 | HCID 44552710 | — |
Reaction Steps
To a mixture of 8-isocyanato-2-(3-(trifluoromethoxy)phenyl)quinoline (0.277 mmol) in toluene (5 mL) was added 2-aminothiazole (0.553 mmol, 55 mg). The mixture was concentrated to dryness, redissolved in pyridine and microwave heated (140° C.×10 min). The reaction mixture was diluted with CH2Cl2, washed with saturate aqueous NaHCO3, water, brine. The organic layer was dried (Na2SO4) and concentrated under reduced pressure. Purification by column chromatography (0% to 100% ethyl acetate in pentane) afforded the desired product. MS (ESI) calcd for C20H13F3N4O2S (m/z): 430.07. found: 431 [M+1].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08685970B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-907ab84e58e04f68bf914c2c98aaff49 |
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| Source note | uspto-grants-2014_04 |
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