Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Cyclosporin A | HCID 5284373 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86691820 | HCID 86691820 | 95% |
Reaction Steps
To a solution of 12 g (10 mmol) of Cyclosporin A (MW: 1202.61) in 40 ml of acetic anhydride (MW: 102.09, d 1.082), 40 ml of pyridine (MW: 79.01, d 0.978) and 0.4 g of 4-N,N-dimethylaminopyridine (MW: 122.17) was added. This solution was stirred for overnight at room temperature, and then the mixture was diluted with 600 ml of ethyl acetate. The mixture was washed with brine, saturated ammonium chloride water solution and with 15% of sodium bicarbonate. The organic phase was dried with sodium sulphate. filtered and evaporated under the reduced pressure. The toluene was added to the mixture until all of pyridine was evaporated to yield the pale yellow solid residue, which was purified by flash chromatography on a silica gel column (100-200 mesh) with eluent of ethyl acetate in haxene (1/3) to give the 11.8 g (9.48 mmol, 95%) of Cyclosporin A-acetate (MW: 1244.65).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09217015B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-db31b0bdbd65484493174d972793ab96 |
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| Source note | uspto-grants-2015_12 |
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