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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 904043Generated: October 30, 2026

pGlu-Ala-Lys(Boc)-Ser-Gln-(D)-Ala-Gly-Ser-Asn-OBut → HCID 131711923, compound

https://huagongshe.com/reaction/904043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantpGlu-Ala-Lys(Boc)-Ser-Gln-(D)-Ala-Gly-Ser-Asn-OButHCID 131711924—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 131711923HCID 131711923—

Reaction Steps

In 5 ml of trifluoroacetic acid is dissolved 500 mg of pGlu-Ala-Lys(Boc)-Ser-Gln-(D)-Ala-Gly-Ser-Asn-OBut and the solution is allowed to stand at room temperature for 40 minutes. The trifluoroacetic acid is distilled off and the residue is precipitated with ether and recovered by filtration. The powdery product is dissolved in 50 ml of water and the solution is 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 0.1 N-acetic acid 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 185 ml through 202 ml are pooled and lyophilized. Yield 170 mg (34%); [α]D27 -50.6° (c=0.42, H2O); Rf4 (Avicel)=0.25; amino acid analysis (acid hydrolyzate); Lys, 1.00(1); Asp, 0.96(1); Ser, 1.77(2), Glu, 2.02(2); Gly, 1.04(1); Ala, 1.95(2); average recovery 75%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04229438
Source datasetuspto-grants-1980_10
ORD IDord-cc03a65845024b6d9345f509708d1966
Source noteuspto-grants-1980_10