HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 904042Generated: October 30, 2026
HCID 131711922, compound → HCID 131711921, compound
https://huagongshe.com/reaction/904042
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 131711922 | HCID 131711922 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 131711921 | HCID 131711921 | — |
Reaction Steps
In 5 ml of trifluoroacetic acid is dissolved 500 mg of pGlu-Ala-Lys(Boc)-Ser-Gln-Gly-(D)-Ala-Ser-Asn-OBut and the mixture is allowed to stand at room temperature. The trifluoroacetic acid 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 run onto 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-aqueous acetic acid and put onto a column of Sephadex LH-20 (2.5×125 cm), elution being carried out with 0.1 N-aqueous acetic acid. The fractions from 186 ml through 206 ml are pooled and lyophilized. Yield 310 mg (62%); [α]D24 -47.3°(c=0.35, H2O); Rf4 (Avicel)=0.24; amino acid analysis (acid hydrolyzate); Lys, 1.08(1); Asp, 1.00(1); Ser, 1.90(2); Glu, 1.93(2); Gly, 1.06(1); Ala, 2.00(2); average recovery 89%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04229438 |
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| Source dataset | uspto-grants-1980_10 |
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| ORD ID | ord-311a272c595e4bbd90061007ffb60838 |
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| Source note | uspto-grants-1980_10 |
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