HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 18396559, compound → HCID 18465745, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 18396559 | HCID 18396559 | — |
| Reactant | HCID 54324685 | HCID 54324685 | — |
| Reactant | HCID 66756783 | HCID 66756783 | — |
| Product | HCID 18465745 | HCID 18465745 | — |
Reaction Steps
was prepared from the acid 212b and (3S,4RS) t-butyl N-(allyloxycarbonyl)-3-amino-4-hydroxy-4-(5,7-dichlorobenzoxazol-2-yl)butanoate (204) by an analogous method as that used for compound 215e to afford a mixture of diastereomers (460 mg, 70%) as a glass: IR (film) 3325, 1725, 1664, 1453, 1399, 1373, 1327, 1274, 1256, 1155; 1H NMR (CDCl3) δ7.57 (1H, m), 7.36 (2H, m), 6.06 (1H, t), 5.29 (2H, m), 4.79 (1H, m), 4.47 (1H, m), 3.23 (1H, m), 2.97 and 2.94(3H combined, 2×s), 2.9-2.4 (4H, m), 2.30 (1H, m), 1.96 (4H, m), 1.41 and 1.37 (9H combined, 2×s). MS ES Da/e 660 (M−1)− Cl35 100%, 662 (M−1) Cl37.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06423840B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-4cabac0b95bf446db8f30733d407b95c |
| Source note | uspto-grants-2002_07 |