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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2219848Generated: November 1, 2026

Acetonitrile → sodium;(E)-7-[3-(4-fluorophenyl)-1-propan-2-ylindol-2-yl]-3,5-dihydroxyhept-6-enoate

https://huagongshe.com/reaction/2219848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantSodium HydroxideHCID 14798—
ReactantFluvastatin methyl esterHCID 13741557—
SolventMethanolHCID 887—
Productsodium;(E)-7-[3-(4-fluorophenyl)-1-propan-2-ylindol-2-yl]-3,5-dihydroxyhept-6-enoateHCID 1676042581.1%

Reaction Conditions

Temperature40 °C

Reaction Steps

Fluvastatin methyl ester (3.0 g) was added to acetonitrile (60 ml) and dissolved by heating the mixture to reflux. The solution was then cooled to about 40° C. and NaOH (1 eq.) dissolved in MeOH (7.5 ml) was added. Turbidity appeared immediately. After 30 minutes an oil residue separated from the mixture. The mixture was heated again to about 55° C. for 3 h to dissolve the oil. The product was isolated by filtration under nitrogen, washed with acetonitrile (40 ml) and dried at 50° C. in a vacuum oven for 24 h to obtain 2.48 g (81.1%) of fluvastatin sodium Form LV.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07414140B2
Source datasetuspto-grants-2008_08
ORD IDord-79fa96aee7224d0995867bf9b418c9f8
Source noteuspto-grants-2008_08