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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 71015Generated: October 28, 2026

2-Amino-2-methyl-1-propanol → 2-Amino-2-methyl-1-propanol

https://huagongshe.com/reaction/71015

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-2-methyl-1-propanolHCID 11807—
ReactantAtorvastatinHCID 60823—
SolventAcetonitrileHCID 6342—
Product2-Amino-2-methyl-1-propanolHCID 11807—
ProductAtorvastatinHCID 60823—
ProductAtorvastatin 2-amino-2-methylpropan-1-olHCID 11541957—

Reaction Steps

The 2-amino-2-methylpropan-1-ol salt of atorvastatin 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 2-amino-2-methylpropan-1-ol was prepared by dissolving 173.08 mg (1.1 equivalents) in acetonitrile (100 mL). The stock solution of atorvastatin free acid was added to the counterion solution with stirring. Seed crystals of the 2-amino-2-methylpropan-1-ol salt were added. Over time, additional acetonitrile was added to aid in stirring (100 mL), and the solid was allowed to stir. After 4 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), and placed in a 25° C. oven under nitrogen to dry for two days to afford atorvastatin 2-amino-2-methylpropan-1-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822703B2
Source datasetuspto-grants-2014_09
ORD IDord-e2d423d9d006489b940e715357376ebd
Source noteuspto-grants-2014_09