HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(3-{[(Benzyloxy)carbonyl]amino}phenoxy)acetic acid → 1-{(2S,3S)-3-[N2-(3-Benzyloxycarbonylaminophenoxy)acetyl-L--asparaginyl]amino-2-hydroxy-4-phenylbutyryl}-N-t-butyl-L-prolinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(3-{[(Benzyloxy)carbonyl]amino}phenoxy)acetic acid | HCID 18957386 | — |
| Reactant | 1-[(2S,3S)-3-L-asparaginylamino-2-hydroxy-4-phenylbutyryl]-N-t-butyl-L-prolinamide hydrochloride | HCID 67722782 | — |
| Product | 1-{(2S,3S)-3-[N2-(3-Benzyloxycarbonylaminophenoxy)acetyl-L--asparaginyl]amino-2-hydroxy-4-phenylbutyryl}-N-t-butyl-L-prolinamide | HCID 86750822 | 50.2% |
Reaction Steps
Following a procedure similar to that described in Example 14, but using 0.45 g (0.91 mmol) of 1-[(2S,3S)-3-L-asparaginylamino-2-hydroxy-4-phenylbutyryl]-N-t-butyl-L-prolinamide hydrochloride and 0.30 g (1.00 mmol) of 3-benzyloxycarbonylaminophenoxyacetic acid, 0.34 g of the title compound were obtained as a colorless powder, melting at 107°-117° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05629406 |
| Source dataset | uspto-grants-1997_05 |
| ORD ID | ord-1594ba3e8e6e495c9513ad7386328805 |
| Source note | uspto-grants-1997_05 |