Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 2733084 | — |
| Reactant | HCID 86699911 | HCID 86699911 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 73294496 | HCID 73294496 | 31% |
Reaction Steps
In a four necked round bottom flask, Et3N (1.4 ml, 10.1 mmol) was added to a solution of (2R,3S)-3-hydroxy-2-{[(3-phenylpropoxy)carbonyl]amino}butanoic acid (0.95 g, 3.38 mmol) in dry CH2Cl2 (40 mL) under argon. After cooling at 0° C., HBTU (1.92 g, 5.07 mmol, 1.5 eq) was added and the mixture stirred 3 h at 0° C., then 16 h at rt. The obtained solid was filtered off and the solvent removed under vacuum. The crude was purified by typical silica gel column chromatography, eluting with Cy/AcOEt (from 95:5 to 60:40). The resulting white solid (0.280 g) was further triturated with cyclohexane to afford the pure title compound (0.240 g, 31%), as white solid. MS (ESI) m/z: 262.27 [M−H]−. Rf=0.29 (Cy/EtOAc 8:2; detection: phosphomolybdic acid). FTIR (cm−1): 3328, 3064, 3030, 2972, 2929, 2859, 1851, 1691, 1542, 1333, 1270, 1130, 1083, 1024, 843, 822, 697. 1H NMR (CDCl3): δ 1.46 (d, 3H); 1.93-2.00 (m, 2H); 2.67-2.71 (m, 2H); 4.09-4.18 (m, 2H); 4.84-4.90 (m, 1H); 5.38-5.48 (m, 2H); 7.11-7.31 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09353075B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-496691d0ee484c86987506ff84aecf61 |
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| Source note | uspto-grants-2016_05 |
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