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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 904041Generated: October 30, 2026

pGlu-(D)-Ala-Lys(Boc)-Ser-Gln-Gly-(D)-Ala-Ser-Asn-OBut → HCID 131711919, compound

https://huagongshe.com/reaction/904041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantpGlu-(D)-Ala-Lys(Boc)-Ser-Gln-Gly-(D)-Ala-Ser-Asn-OButHCID 131711920—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 131711919HCID 131711919—

Reaction Steps

In 2 ml of trifluoroacetic acid is dissolved 250 mg of pGlu-(D)-Ala-Lys(Boc)-Ser-Gln-Gly-(D)-Ala-Ser-Asn-OBut and the solution is allowed to stand at room temperature for 60 minutes. The solvent is distilled off and the residue is precipitated with ether and recovered by filtration. The resulting powders are dissolved in 50 ml of water and passed through a column of Amberlite IRA-410 (acetate-form) (2×5 cm). The effluent is combined with washings and lyophilized. The powdery lyophilizate is dissolved in a small amount of water and put onto a column of Sephadex LH-20 (2.5×125 cm), elution being carried out with 0.1 N-acetic acid. The fractions from 182 ml through 218 ml are pooled and lyophilized. Yield 86 mg (34%); [α]D23 -6.0°(c=0.25, water); Rf4 =0.23; amino acid analysis (as hydrolyzed with HCl): Lys, 0.97(1); Asp, 0.97(1); Ser, 1.80(2); Glu, 2.07(2); Gly, 1.00(1); Ala, 1.93(2); average recovery 82%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04229438
Source datasetuspto-grants-1980_10
ORD IDord-2cbee32a21e0447a888ed3580ba800b8
Source noteuspto-grants-1980_10