HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → Methyl 2-[3-(4-fluoro-3-thiophen-2-ylphenyl)ureido]-2-methylpropionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl 3-isocyanato-2-methylpropanoate | HCID 13063727 | — |
| Reactant | 4-Fluoro-3-(thiophen-2-yl)aniline | HCID 57829334 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 2-[3-(4-fluoro-3-thiophen-2-ylphenyl)ureido]-2-methylpropionate | HCID 57829328 | — |
Reaction Steps
According to process “A′”, 0.12 g of the trifluoroacetic acid salt of compound 267.4 was dissolved at room temperature in 5 ml of dry tetrahydrofuran, admixed with 0.17 ml of triethylamine and then admixed dropwise with a solution of 0.10 g of methyl isocyanatomethylpropionate in 2 ml of dry tetrahydrofuran. The mixture was stirred at room temperature for 2 hours. For workup, the mixture was concentrated under reduced pressure, and the residue was stirred with water, filtered, washed with water and dried. Methyl 2-[3-(4-fluoro-3-thiophen-2-ylphenyl)ureido]-2-methylpropionate (267.3) was obtained. Molecular weight 336.39 (C16H17FN2O3S); retention time Rt=1.46 min. [F]; MS (ESI): 337.05 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07759366B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-1116b2eebb9949b598d40de9eade8f96 |
| Source note | uspto-grants-2010_07 |