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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732525Generated: October 30, 2026

Water → L-Pyroglutamyl-L-methionyl-L-alanyl-L-valyl-L-lysine

https://huagongshe.com/reaction/1732525

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
ReactantSulfoniumHCID 3015009—
Reactantt-Butyloxycarbonyl-L-glutaminyl-L-methionyl-L-alanyl-L-valyl-Nepsilon-benzyloxycarbonyl-L-lysine benzyl esterHCID 86737376—
CatalystPd barium sulfateHCID 16218511—
SolventAcetic AcidHCID 176—
SolventDimethylformamideHCID 6228—
ProductL-Pyroglutamyl-L-methionyl-L-alanyl-L-valyl-L-lysineHCID 22813237—

Reaction Steps

A sample of the protected 5-peptide XXIII (0.50 g, 0.55 mmole) was dissolved in DMF (60 ml), H2O (6 ml), DIEA (6 ml) and 10% Pd/BaSO4 (0.10 g) were added and the mixture hydrogenated for 8 hr. On tlc a single spot (RfC, 0.45; RfL, 0.75) was observed. The black solution was filtered on a layer of Celite, the latter washed with DMF and the filtrates evaporated in vacuo to dryness. The residue was dissolved in TFA (20 ml) containing acetyl-DL-methionine n-butyl ester (1.0 g) and kept at room temperature for 1/2 hr. The TFA was removed in vacuo and the residue dissolved in a mixture of EtOAc (20 ml) and H2O (20 ml). The aqueous layer was extracted twice with EtOAc (20 ml each), filtered and lyophilized to give a white powder, 0.40 g. In system C the spot remained near the origin; RfM, 0.45. Trace amounts of impurities, probably the pyroglutamyl derivative and the sulfonium salt could also be detected. A sample (0.10 g) was dissolved in AcOH (ca 2 ml) and heated to boiling for 3 min. After cooling the product was precipitated with ether (20 ml). The pyroglutamyl derivative was collected, washed with ether: 80 mg; m.p. 238°-242° C.; RfC, 0.10; RfM, 0.60. Glu, 0.98; Ala, 0.99; Val, 1.01; Met, 0.96.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04237046
Source datasetuspto-grants-1980_12
ORD IDord-0dca89cec27c47f1a8364f662a2a6eb1
Source noteuspto-grants-1980_12