Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 23119177 | HCID 23119177 | — |
| Reactant | HCID 57887225 | HCID 57887225 | — |
| Product | HCID 57887232 | HCID 57887232 | — |
Reaction Steps
4-[2-Fluoro-3-(1-methyloxyhexyl)phenyl]thiazol-2-ylamine (460 mg) and methyl (Z)-3-(4-bromo-2,6-difluorophenyl)-2-methyloxyacrylate (462 mg), and dichlorobistriphenylphosphinepalladium (150 mg) were dissolved in DMF (6 mL). Triethylamine (0.84 mL) was added into the mixture, and the reaction mixture was stirred under carbon monoxide atomosphere at 85° C. for 16 h. Water added into the reaction mixture, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with water, and brine, dried over magnesium sulfate, evaporated. The obtained residue was purified by Colum chromatography (hexane:ethyl acetate=4:1) to obtain the compound (24) 630 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07601746B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-2b0f42a615234deeb86f233878902e76 |
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| Source note | uspto-grants-2009_10 |
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