HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Cbz-L-2-amino-4-sulfamoylbutyric acid → (4S)-1-{(2S,3S)-3-[2(S)-Benzyloxycarbonylamino-4-sulfamoylbutyryl]amino-2-hydroxy-4-phenylbutyryl}-4-chloro-N-t-butyl-L-prolinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Cbz-L-2-amino-4-sulfamoylbutyric acid | HCID 20055593 | — |
| Reactant | (4S)-1-[(2S,3S)-3-amino-2-hydroxy-4-phenylbutyryl]-4-chloro-N-t-butyl-L-prolinamide | HCID 22872716 | — |
| Product | (4S)-1-{(2S,3S)-3-[2(S)-Benzyloxycarbonylamino-4-sulfamoylbutyryl]amino-2-hydroxy-4-phenylbutyryl}-4-chloro-N-t-butyl-L-prolinamide | HCID 22872715 | 77.6% |
Reaction Steps
Following a procedure similar to that described in Example 66, but using 122 mg (0.32 mmol) of (4S)-1-[(2S,3S)-3-amino-2-hydroxy-4-phenylbutyryl]-4-chloro-N-t-butyl-L-prolinamide [prepared as described in Preparation 21(b)] and 100 mg (0.32 mmol) of (S)-2-benzyloxycarbonylamino-4-sulfamoylbutyric acid, 169 mg of the title compound were obtained as a colorless powder, melting at 115°-122° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05629406 |
| Source dataset | uspto-grants-1997_05 |
| ORD ID | ord-95561927527c4b05b0c313c82af5a052 |
| Source note | uspto-grants-1997_05 |