Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | Sirolimus | HCID 5284616 | — |
| Edukt | 5-Methyl-2,2-diphenyl-1,3-dioxane-5-carboxylic acid | HCID 52931763 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Temsirolimus | HCID 6918289 | — |
Reaktionsschritte
(189 mg) of 31-trimethyl silyl-42-ester of rapamycin with 5-methyl-2,2-diphenyl-1,3-dioxane-5-carboxylic acid [IId10] was dissolved in 2.8 ml THF and cooled to 0-5° C. Into the reaction mass 0.52 ml 2N sulphuric acid was added and stirred at 25-30° C. for 24 hrs. Then 2 ml THF and 0.52 ml 2 N sulphuric acid was added and stirred at 25-30° C. for 76 hrs. It was then concentrated on rotavapour, residue was dissolved in 2 ml ethyl acetate, and 2-3 drop perchloric acid (HClO4) diluted with 1 ml water was added. The reaction mixture was stirred at 25-30° C. for 24 hrs and reaction mass was dumped into water, and extracted with ethyl acetate. The layers were separated and washed the organic layer with 10% sodium bicarbonate solution and then water. It was dried over sodium sulfate, concentrated on rotavapor to obtain yellow colored oily compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08754207B2 |
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| Quelldatensatz | uspto-grants-2014_06 |
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| ORD ID | ord-1b08d1152dc2441b8cdd805ff4f653f5 |
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| Quellennotiz | uspto-grants-2014_06 |
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