HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395908Generated: October 30, 2026
Methanesulfonic Acid → Nelfinavir Mesylate
https://huagongshe.com/reaction/395908
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Nelfinavir | HCID 64143 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Nelfinavir Mesylate | HCID 64142 | — |
Reaction Steps
Nelfinavir free base (10.2 kg, 18.0 mol) and 24 L of tetrahydrofuran were added to a 100L 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06605721B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-34c6e81b03ca44ba9a4cc6c353d0b35c |
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| Source note | uspto-grants-2003_08 |
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