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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247109Generated: October 31, 2026

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

https://huagongshe.com/reaction/2247109

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 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 40EC 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 55EC for 3 h to dissolve the oil. The product was isolated by filtration under nitrogen, washed with acetonitrile (40 ml) and dried at 50EC 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 numberUS07687642B2
Source datasetuspto-grants-2010_03
ORD IDord-19d4d219cb7d4865befdc4f26470953e
Source noteuspto-grants-2010_03