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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636083Generated: October 30, 2026

Methanesulfonic Acid → Nelfinavir Mesylate

https://huagongshe.com/reaction/1636083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantNelfinavirHCID 64143—
SolventTetrahydrofuranHCID 8028—
ProductNelfinavir MesylateHCID 64142—

Reaction Steps

Nelfinavir free base (10.2 kg, 18.0 mol) and 24 L of tetrahydrofuran were added to a 100 L reactor. Methanesulfonic acid (1.8 kg, 18.48 mol) also was added to the reactor. The reactor was stirred until all solids dissolved, and then the solution was filtered into a 100 gallon polypropylene tank containing 306 L methyl t-butyl ether or diethyl ether that was rapidly stirring. After stirring for 2 hours, the 100 gallon tank contents were filtered, washed with 17 L of methyl t-butyl ether or diethyl ether, and pulled as dry as possible. The solid was transferred to a rotocone drier and dried in a vacuum oven at 60-65° C. (at least 26 in. Hg or higher vacuum) for 12-72 hours or until the methyl t-butyl ether or diethyl ether content of the dried solid was below 1%. If necessary, the drier contents could be milled in a Fitzmill grinder to accelerate drying. Typical yields of nelfinavir mesylate range from 9 to 11 kg. (76%-92% theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06512135B2
Source datasetuspto-grants-2003_01
ORD IDord-33ec9f9e9ae045b4aa714f5243857cc0
Source noteuspto-grants-2003_01