Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Methylurea | HCID 11719 | — |
| Reactant | Methanol, magnesium salt (2:1) | HCID 164537 | — |
| Reactant | 3-Cyclopentyl-2-(4-trifluoromethylsulfanylphenyl)propionic acid methyl ester | HCID 46221383 | — |
| Product | HCID 12044457 | HCID 12044457 | 18.1% |
Reaction Steps
3-Cyclopentyl-2-(4-trifluoromethylsulfanyl-phenyl)propionic acid methyl ester (210.1 mg, 0.63 mmol) and methyl urea (140.5 mg, 1.90 mmol) were treated with a solution of magnesium methoxide in methanol (7.4 wt %, 3.6 mL, 2.53 mmol). The resulting reaction mixture was then heated under reflux for 64 h. The reaction mixture was allowed to cool to 25° C. and then filtered through celite. The celite was thoroughly washed with ethyl acetate until the solvent passing through the celite showed absence of desired product by thin layer chromatography. The filtrate was concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 70-230 mesh, 3/1 hexanes/ethyl acetate) afforded 1-[3-cyclopentyl-2-(4-trifluoromethylsulfanyl-phenyl)-propionyl]-3-methyl urea (42.7 mg, 18%) as a white solid: mp 144-145° C.; EI-HRMS m/e calcd for C17H21F3N2O2S (M+) 374.1276, found 374.1270.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06528543B1 |
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| Source dataset | uspto-grants-2003_03 |
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| ORD ID | ord-6d037e26d2b441309fd1b7dcde994e3e |
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| Source note | uspto-grants-2003_03 |
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