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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1738607Generated: October 28, 2026

Methanol → Nelfinavir Mesylate

https://huagongshe.com/reaction/1738607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantMethanesulfonic AcidHCID 6395—
ReactantNelfinavirHCID 64143—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Solventtert-Butyl methyl etherHCID 15413—
ProductNelfinavir MesylateHCID 64142—

Reaction Steps

Nelfinavir free base is slurried or dissolved in a suitable solvent (such as THF, methanol, or ethanol). THF is the preferred solvent. A molar equivalent amount of methanesulfonic acid is added, and the mixture is stirred until all solids dissolve. The solution is added to several volumes of an antisolvent (such as methyl t-butyl ether, diethyl ether, hexanes, or heptanes) that is rapidly stirring. Diethyl ether is the preferred antisolvent. After stirring, the mixture is filtered and washed with antisolvent. The solid is dried in a vacuum oven to yield nelfinavir mesylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962725
Source datasetuspto-grants-1999_10
ORD IDord-ce2468c1868942218e53f005c0375010
Source noteuspto-grants-1999_10