HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 2-{2-[2-(1-Carboxy-3-methyl-butylcarbamoyl)-4-methoxy-phenyldisulfanyl]-5-methoxybenzoylamino}-4-methyl-pentanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Anisole | HCID 7519 | — |
| Reactant | HCID 76479708 | HCID 76479708 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-{2-[2-(1-Carboxy-3-methyl-butylcarbamoyl)-4-methoxy-phenyldisulfanyl]-5-methoxybenzoylamino}-4-methyl-pentanoic acid | HCID 6917072 | 34.7% |
Reaction Steps
This compound was prepared according to the procedure described in Example 50 using [S-(R*,R*)]-2-[2-[2-(1-tert-butoxycarbonyl-3-methyl-butylcarbamoyl)-4-methoxy-phenyldisulfanyl]-5-methoxy-benzoylamino]-4-methyl-pentanoic acid tert-butyl ester(2.4 g, 3.4 mmol) from Example 31, 25 mL dichloromethane, 25 mL trifluoroacetic acid and 2.5 mL anisole. The crude product was recrystallized from methanol/water to afford 0.7 g of the title compound, mp 168°-169° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05668291 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-9294b019079d43ad9755f0b716855a9c |
| Source note | uspto-grants-1997_09 |