HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Hydroxybenzotriazole → t-Butyloxycarbonyl-L-methionyl-L-alanyl-L-valyl-Nepsilon-benzyloxycarbonyl-L-lysine benzyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Trifluoroacetate | HCID 84468 | — |
| Reactant | Boc-Met-ONp | HCID 7021880 | — |
| Reactant | t-Butyloxycarbonyl-L-alanyl-L-valyl-Nepsilon-benzyloxycarbonyl-L-lysine benzyl ester | HCID 131711964 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | t-Butyloxycarbonyl-L-methionyl-L-alanyl-L-valyl-Nepsilon-benzyloxycarbonyl-L-lysine benzyl ester | HCID 86737377 | — |
Reaction Steps
Partial deprotection of compound XXI (3.4 g, 5.3 mmole) was carried out as described in the previous paragraph. The trifluoroacetate salt (RfC, 0.75) was acylated in DMF (50 ml) with Boc-L-Met-ONp (2.18 g, 5.9 mmole, Bachem) in the presence of DIEA (1.9 ml, 12 mmole) and HOBt (0.9 g, 5.9 mmole). After 4 hr at room temperature the reaction was complete. Evaporation of most of the solvent in vacuo was followed by trituration with EtOAc. The precipitate was washed with EtOAc, with ether and dried: 3.8 g (93%); m.p. 169°-171° C., [α]D24 -21.5° (c 1.2, DMF) RfK, 0.65; RfI, 0.52.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04237046 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-83288b81c18f488c859c673fe04e5fbf |
| Source note | uspto-grants-1980_12 |