HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 12802420, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 12802418 | HCID 12802418 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Acetic acid 10-acetoxymethyl-anthracen-9-ylmethyl ester | HCID 613145 | — |
| Product | HCID 12802420 | HCID 12802420 | — |
Reaction Steps
In 50 ml of MeOH is dissolved 250 mg of Z-Tyr-(D)-Ala-Gly-Phe-NH-NH2, and following addition of 0.1 ml of acetic acid, catalytic reduction is carried out with palladium black as the catalyst. The catalyst is filteredoff, the filtrate is dissolved in a small amount of 1 N-aqueous acetic acidand the solution is put on a column of Sephadex LH-20(2.5×120 cm). Elution is carried out with 1 N-aqueous acetic acid and fractions from 310ml through 335 ml are pooled and lyophilized. 95 mg (38%); [α]D22 +20.5° (c=0.2, MeOH); Rf2 =0.22; amino acid analysis (hydrolyzed with HCl): Gly, 1.00; Ala, 1.05; Tyr, 0.89; Phe,1.01; mean recovery rate 81%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04277394 |
| Source dataset | uspto-grants-1981_07 |
| ORD ID | ord-eb01311755f4442dbc4e8262a334c04e |
| Source note | uspto-grants-1981_07 |