Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Diethyl cyanophosphonate | HCID 76257 | — |
| Reactant | 4-(Trifluoromethyl)benzylamine | HCID 76804 | — |
| Reactant | HCID 59218967 | HCID 59218967 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Water TFA acetonitrile | HCID 22145617 | — |
| Product | HCID 59218923 | HCID 59218923 | — |
Reaction Steps
12 mg of 2-Methoxy-5-[3-(methoxycarbonyl)phenyl]benzoic acid and 9 mg of 4-trifluoromethylbenzylamine were dissolved in 0.2 ml of N,N-dimethylformamide, 9 ml of diethyl cyanophosphonate and 50 ml of triethylamine were added thereto, and the mixture was stirred at room temperature for 1 hour. Ethyl acetate was added to the reaction mixture which was then washed with water. The organic layer was evaporated, and the residue was dissolved in 0.4 ml of ethanol. 0.1 ml of 5N sodium hydroxide was added thereto, and the mixture was stirred at room temperature for 1 hour. 1 N hydrochloric acid was added to the reaction mixture which was then extracted with ethyl acetate. The organic layer was evaporated, and the residue was purified by HPLC using a reverse phase system column and a water-acetonitrile-trifluoroacetic acid eluent, to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07687664B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-74cf0548c329468696dc40461e08b348 |
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| Source note | uspto-grants-2010_03 |
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