HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrophenyl formate → HCID 131720515, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrophenyl formate | HCID 74628 | — |
| Reactant | HCID 131720516 | HCID 131720516 | — |
| Reactant | HCID 131720517 | HCID 131720517 | — |
| Product | HCID 131720515 | HCID 131720515 | — |
Reaction Steps
140 mg of 5(S)-amino-4(S)-hydroxy-2(R),7,7-trimethyl-8-[2(R,S)-methylaminocarbonyl-3,4-dihydro-2H-1,4-benzoxazin-4-ylcarbonyl]-octanoic acid (N-butyl)amide (Example 28)) are reacted with 100 mg of 4-nitrophenyl formate in a manner analogous to that described in Example 17): Rf (S)=0.33; FAB-M S: (M+H)+ =519.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05719141 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-79cbc788f4684794be8ab5521be48219 |
| Source note | uspto-grants-1998_02 |