Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 23119177 | HCID 23119177 | — |
| Reactant | HCID 69065387 | HCID 69065387 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 74018211 | HCID 74018211 | — |
Reaction Steps
To a DMF (6 mL) solution of 4-[2-fluoro-3-(1-methyloxyhexyl)phenyl]thiazol-2-ylamine (318 mg), 3-(4-bromo-2,6-difluoropheny)-2-methylacrylic acid ethyl ester (300 mg), and dichlorobistriphenylphosphinepalladium (36 mg) was added triethylamine (0.43 mL). The reaction mixture was stirred under carbon monoxide atomosphere at 85° C. for 16 h. Water was poured into the reaction mixture, and the reaction mixture extracted with ethyl acetate, and the organic layer was washed with water, and brine, dried over magnesium sulfate, and evaporated. The obtained residue was purified by Colum chromatography (hexane:ethyl acetate=4:1) to obtain the compound (20) 500 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07601746B2 |
|---|
| Source dataset | uspto-grants-2009_10 |
|---|
| ORD ID | ord-bce18521165041b7a5526042a6f8c3c4 |
|---|
| Source note | uspto-grants-2009_10 |
|---|