Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Diethyl cyanophosphonate | HCID 76257 | — |
| Reactant | 3-Cyano-5-[(dipropylamino)carbonyl]Benzoic Acid | HCID 22593638 | — |
| Reactant | HCID 58759815 | HCID 58759815 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86585855 | HCID 86585855 | — |
Reaction Steps
To a mixture of 3-cyano-5-[(dipropylamino)carbonyl]benzoic acid (IX/XXXII, PREPARATION 7, 0.086 g, 0.314 mmol) and tert-butyl (2R,3S)3-amino-2-hydroxy4-phenylbutyl(3-methoxybenzyl)carbamate (XXXV, EXAMPLE 584, 0.126 g, 0.314 mmol) in dichloromethane (0.3 mL) is added diethylcyanophosphonate (0.062 g, 0.330 mmol) and triethylamine (0.032 g, 0.316 mmol). The mixture is stirred at 20–25 degrees for 65 hours and then partitioned between dichloromethane and saturated aqueous sodium bicarbonate. The organic phase is separated and dried over sodium sulfate and concentrated. The residue is chromatographed (silica gel, 20 mL; methanol/dichloromethane, 5/95) to give several mixed fractions, which are combined and rechromatographed (silica gel; acetone/hexane, 20/80) to give the title compound, MS (ESI+) for C35H48N4O6 M/z 657.6 (M+H)+=657.6; (M+Na)=679.5 and (M—C4H9O2)=557.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07214715B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-9b3b59605edc4b55b96911347bfcb071 |
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| Source note | uspto-grants-2007_05 |
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