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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254880Generated: October 26, 2026

Acetonitrile → Benzathine

https://huagongshe.com/reaction/254880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantAtorvastatinHCID 60823—
SolventWaterHCID 962—
ProductBenzathineHCID 8793—
ProductAtorvastatinHCID 60823—
Product3-Phenylpropane-1,2-diamineHCID 413434—

Reaction Steps

The benzathine salt of atorvastatin (Form B) was synthesized by preparing a stock solution of the free acid of atorvastatin (U.S. Pat. No. 5,273,995) in acetonitrile (1 g in 40 mL of ACN). A solution of N,N′-bis(phenylmethyl-1,2-ethanediamine (benzathine) was prepared by dissolving 220.64 mg (0.5 equivalents) in acetonitrile (80 mL) and water (20 mL). The stock solution of atorvastatin free acid was added to the counterion solution with stirring. After 2 days of stirring at ambient temperature, the solids were isolated by vacuum filtration using a Buchner funnel fitted with a paper filter (#2 Whatman). The solids were rinsed with acetonitrile (75 mL) to afford atorvastatin benzathine Form B. Note that this procedure is the same as above except that the sample was not oven dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875731B2
Source datasetuspto-grants-2011_01
ORD IDord-6b243acc9cae42fe9d9fb5e64fb91417
Source noteuspto-grants-2011_01