Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | methyl 3-([(2S)-2-[(benzyloxy)carbonyl]amino-3-(1H-4-imidazolyl)propanoyl]-2-[(2-methyl-2-phenylpropyl)amino]-2-oxoethylamino)propanoate | HCID 178500811 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178449518 | HCID 178449518 | 27% |
Reaction Steps
The product from Example 4 (0.30 g, 0.53 mmol) was dissolved in tetrahydrofuran (10 mL), methanol (10 mL) and water (1 mL). Sodium hydroxide (42 mg, 1.05 mmol) was added and the reaction was stirred overnight at room temperature. The solution was concentrated in vacuo and the residue taken up in 0.1 M NaPO4 buffer (100 mL). The pH was brought to 6 by the addition of 1N HCl. The product was extracted three times with ethyl acetate. The ethyl acetate was washed twice with brine, dried over MgSO4, filtered and concentrated in vacuo. Purification was carried out via reversed-phase HPLC (0.1 % trifluoroacetic acid in acetonitrile and 0.1% aqueous trifluoroacetic acid as eluent; C-18 column) to give a white powder; 0.078 g (27% yield). MS-APCI: M+1=550.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06369034B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-35fe5d5dcb82491c945cda8a1ce8e0f2 |
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| Source note | uspto-grants-2002_04 |
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