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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505820Generated: November 1, 2026

Acetic Anhydride → HCID 86691820, compound

https://huagongshe.com/reaction/1505820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantCyclosporin AHCID 5284373—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductHCID 86691820HCID 8669182095%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09217015B2
Source datasetuspto-grants-2015_12
ORD IDord-db31b0bdbd65484493174d972793ab96
Source noteuspto-grants-2015_12