Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Tolyl isocyanate | HCID 69194 | — |
| Reactant | HCID 23511692 | HCID 23511692 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 23511749 | HCID 23511749 | 42% |
Reaction Steps
To a stirred solution of ethyl 4-amino-2,3-difluorophenylacetate (323 mg, 1.5 mmol) in DMF (8 mL), were added triethylamine (0.209 ml, 1.5 mmol) and 2-methylphenyl isocyanate (0.372 ml, 3.0 mmol) at rt. The stirring was continued for 48 hour at 80° C. The reaction mixture was evaporated in vacuo, and the solid was suspended to n-hexane. The solid was collected through filtration. The solid was dissolved in THF-MeOH (1:1, v/v, 20 mL), and was added 4M NaOH (10 mL) at rt. The stirring was continued for 18 hours at rt. The reaction was poured into 1M HCl, and the resulting precipitate was collected through filtration. The solid was recrystallized with CHCl3-n-hexane to give 4-[(2-methylphenyl)ureido]-2,3-difluorophenylacetic acid (200 mg, 42%) as a white solid. 1H-NMR (CDCl3) δ 2.30 (s, 3 H), 3.35 (s, 2 H), 6.98 (m, 1 H), 7.04 (m, 1 H), 7.18 (d, J=7.3 Hz, 2 H), 7.69 (d, J=8.1 Hz, 1 H), 7.90 (m, 1 H); MS (FAB) m/z 321 (M++1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07179819B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-f42f528a16da4e3b9ccb589522f7e410 |
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| Source note | uspto-grants-2007_02 |
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