Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | phenyl N-(1,3-thiazol-2-yl)carbamate | HCID 651148 | — |
| Reactant | Tetrahydrofuran ethyl acetate | HCID 21939870 | — |
| Reactant | HCID 67201867 | HCID 67201867 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 86591479 | HCID 86591479 | 54.51% |
Reaction Steps
After dissolving 4-(4-aminophenoxy)-6-cyano-7-(((2R)-3-(diethylamino)-2-hydroxypropyl)oxy)quinoline (105 mg, 0.2583 mmol) in dimethylsulfoxide (1 ml), there was added phenyl (thiazol-2-yl)carbamate (60 mg, 0.2712 mmol), and the mixture was heated and stirred at 85° C. for 40 minutes. After cooling to room temperature, water was added to the reaction solution, extraction was performed with ethyl acetate-tetrahydrofuran, and the extract was washed with saturated brine and dried over anhydrous sodium sulfate. Upon distilling off the solvent, the residue was dissolved in acetone and diluted with diethyl ether, and the precipitate was washed with diethyl ether and blow-dried to obtain the title compound (75 mg, 0.1408 mmol, 54.51%) as a light yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07612092B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-6bb1f7274b7143f3b72a3500172eb2a4 |
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| Source note | uspto-grants-2009_11 |
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