Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 86608790 | HCID 86608790 | — |
| Reactant | HCID 161369107 | HCID 161369107 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 178472285 | HCID 178472285 | 19.5% |
Reaction Steps
2-(3-aminophenyl)-3-di(ethoxy)phosphinoylpropanoic acid ethyl ester (350.0 mg, 0.96 mmol), N,N′-di(t-butoxycarbonyl)guanidine triflate (375 mg, 0.96 mmol), chloroform (10 mL) and triethylamine (133.4 mL, 0.96 mmol) were combined in a 25 ml flask and stirred at 50° C. for 27 hours. The solvents were evaporated. The resulting residue was dissolved in acetonitrile/water (8 mL) and purified by preparative chromatography. The fractions were combined and evaporated to an oil, which was dried under high vacuum for 48 hours to give 107 mg of 2-(3-N,N′-di(t-butoxycarbonyl)-guanidinophenyl)-3-di(ethoxy)phosphinoylpropanoic acid ethyl ester, which was used in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07528173B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-fed12a247cb3470d8dbd2e52f803b377 |
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| Source note | uspto-grants-2009_05 |
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