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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732523Generated: November 2, 2026

1-Hydroxybenzotriazole → t-Butyloxycarbonyl-L-methionyl-L-alanyl-L-valyl-Nepsilon-benzyloxycarbonyl-L-lysine benzyl ester

https://huagongshe.com/reaction/1732523

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantTrifluoroacetateHCID 84468—
ReactantBoc-Met-ONpHCID 7021880—
Reactantt-Butyloxycarbonyl-L-alanyl-L-valyl-Nepsilon-benzyloxycarbonyl-L-lysine benzyl esterHCID 131711964—
SolventDimethylformamideHCID 6228—
Productt-Butyloxycarbonyl-L-methionyl-L-alanyl-L-valyl-Nepsilon-benzyloxycarbonyl-L-lysine benzyl esterHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04237046
Source datasetuspto-grants-1980_12
ORD IDord-83288b81c18f488c859c673fe04e5fbf
Source noteuspto-grants-1980_12