Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | L-Tyrosine | HCID 6057 | — |
| Reactant | HCID 178418600 | HCID 178418600 | — |
| Reactant | HCID 178491774 | HCID 178491774 | — |
| Solvent | HCID 67440411 | HCID 67440411 | — |
| Product | HCID 178512890 | HCID 178512890 | — |
Reaction Steps
In 5 ml of mixed solution of trifluoroacetic acid-thioanisole (9:1) was dissolved 400 mg of Boc-Tyr-Arg(Mtr)OH and the resulting mixture was allowed to stand at room temperature for 2 hours. The trifluoroacetic acid was distilled off under reduced pressure, ether was added to the residue and the resulting precipitate was collected by filtration. The precipitate was dissolved in a small amount of water, passed through a column (1×10 cm) of Amberlite IRA-410 (acetate-form) and lyophilized. The lyophilizate was dissolved in a small amount of water, chromatographed on a carboxymethyl-cellulose column (2.2×8 cm) and eluted by the linear gradient method using water (300 ml) and 0.1 M ammonium acetate (300 ml). The fractions from 100 to 150 ml were pooled and lyophilized. Yield 175 mg, [α]D21 -17.4° (c=0.5, H2O); amino acid analysis (acid hydrolysis): Arg 1.00(1), Tyr 0.94(1); average recovery 86.5%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04368150 |
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| Source dataset | uspto-grants-1983_01 |
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| ORD ID | ord-24b442b815774101a44308afbfcf6864 |
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| Source note | uspto-grants-1983_01 |
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