Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Salinomycin | HCID 3085092 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 20-Deoxysalinomycin | HCID 198464 | — |
| Product | Salinomycin | HCID 3085092 | — |
Reaction Steps
Fifty grams of the crude salinomycin powder is dissolved in ethyl acetate and applied to column (50 g of active almina, commercial product of Wako Junyaku Co.). After washing the column with one liter of ethyl acetate, salinomycin and SY-1 are eluted with a 100:5 mixture of ethyl acetate-methanol solution. The fractions containing salinomycin and SY-1 are combined and concentrated. The concentrate is diluted in 50 ml of chloroform-methand solution (100:2) and applied to the column of 300 g silica gel (Wakogel-200, Wako Junyaku Co.) packed in the same solvent mixture. Elution is carried out with the same solvent mixture to give pure salinomycin fraction and pure SY-1 fraction. Each fraction is concentrated and crystallized from acetone-water solution to give 5 g of salinomycin and 30 mg of SY-1 in pure crystals, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04212942 |
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| Source dataset | uspto-grants-1980_07 |
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| ORD ID | ord-0acb7dd2d1d54f129c3428532d539181 |
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| Source note | uspto-grants-1980_07 |
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