HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrophenyl formate → HCID 131720513, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrophenyl formate | HCID 74628 | — |
| Reactant | HCID 131720510 | HCID 131720510 | — |
| Product | HCID 131720513 | HCID 131720513 | — |
Reaction Steps
195 mg of 5(S)-amino-4(S)-hydroxy-2(R),7,7-trimethyl-8-[2(R,S)-methoxycarbonyl-3,4-dihydro-2H-1,4-benzothiazin-4-ylcarbonyl]-octanoic acid (N-butyl)amide (Example 18)) are reacted with 128 mg of 4-nitrophenyl formate in a manner analogous to that described in Example 17) and the product is purified over 30 g of silica gel (mobile phase M). The title compound is obtained as a yellowish-coloured solid: Rf (N)=0.20; FAB-MS: (M+H)+ =536.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05719141 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-a0094474144045658ecad9eea724d123 |
| Source note | uspto-grants-1998_02 |