Methanol → Nelfinavir Mesylate

HRID 1636082Notes

Reaction equation

HRID 1636082 reaction equation
[CH3:1][C:2]1[C:7]([OH:8])=[CH:6][CH:5]=[CH:4][C:3]=1[C:9]([NH:11][C@H:12]([C@H:21]([OH:40])[CH2:22][N:23]1[C@H:32]([C:33]([NH:35][C:36]([CH3:39])([CH3:38])[CH3:37])=[O:34])[CH2:31][C@H:30]2[C@H:25]([CH2:26][CH2:27][CH2:28][CH2:29]2)[CH2:24]1)[CH2:13][S:14][C:15]1[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=1)=[O:10].CO.[CH3:43][S:44]([OH:47])(=[O:46])=[O:45]>C(OCC)C.C(OC)(C)(C)C.C1COCC1.C(O)C>[CH3:1][C:2]1[C:7]([OH:8])=[CH:6][CH:5]=[CH:4][C:3]=1[C:9]([NH:11][C@H:12]([C@H:21]([OH:40])[CH2:22][N:23]1[C@H:32]([C:33]([NH:35][C:36]([CH3:38])([CH3:37])[CH3:39])=[O:34])[CH2:31][C@H:30]2[C@H:25]([CH2:26][CH2:27][CH2:28][CH2:29]2)[CH2:24]1)[CH2:13][S:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)=[O:10].[CH3:43][S:44]([OH:47])(=[O:46])=[O:45]

Participants

8

Reactant 3

HCID 887MethanolHCID 6395Methanesulfonic AcidHCID 64143Nelfinavir

Product 1

HCID 64142Nelfinavir Mesylate

Reagents, catalysts & solvents 4

HCID 702EthanolSolventHCID 3283Diethyl EtherSolvent2×HCID 8028TetrahydrofuranSolvent2×HCID 15413tert-Butyl methyl etherSolvent

Procedure

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.

Workup

  1. dissolutiondissolve
  2. stirringis rapidly stirring
  3. stirringAfter stirring
  4. filtrationthe mixture is filtered
  5. washwashed with antisolvent
  6. customThe solid is dried in a vacuum oven

Sources & evidence

ORD record
ord-7156e9434bbc4077ac3764646a178b14
Source dataset
uspto-grants-2003_01
Patent number
US06512135B2

Reaction notes

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