Sodium Carbonate → Voriconazole

HRID 1099531Notes

Reaction equation

HRID 1099531 reaction equation
[CH3:1][C@H:2]([C@@:10]([OH:25])([C:17]1[CH:18]=[CH:19][C:20]([F:24])=[CH:21][C:22]=1[F:23])[CH2:11][N:12]1[N:16]=[CH:15][N:14]=[CH:13]1)[C:3]1[N:8]=[CH:7][N:6]=[CH:5][C:4]=1[F:9].[C@@]12(CS([O-])(=O)=O)C(C)(C)C(CC1)CC2=O.C([O-])([O-])=O.[Na+].[Na+]>O>[CH3:1][C@H:2]([C@@:10]([OH:25])([C:17]1[CH:18]=[CH:19][C:20]([F:24])=[CH:21][C:22]=1[F:23])[CH2:11][N:12]1[N:16]=[CH:15][N:14]=[CH:13]1)[C:3]1[N:8]=[CH:7][N:6]=[CH:5][C:4]=1[F:9]

Participants

4

Reactant 2

HCID 10340Sodium CarbonateHCID 86626425Voriconazole (1R)-(-)-10-camphorsulfonate

Product 1

HCID 71616VoriconazoleYield 86.25%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Conditions

Temperature
22.5 °C

Procedure

Voriconazole (1R)-(−)-10-camphorsulfonate (4 g, 6.88 mmol, enantiomeric purity 98.52) was suspended in deionised water (200 ml) and treated with aqueous 10% w/v Na2CO3 (7.29 ml, 6.88 mmol) at 45-55° C. for 3 hours and 30 minutes. The suspension was cooled down to 20-25° C., stirred for 15 minutes and filtered. The cake was washed with deionised water (2×10 ml). The solid was dried at 50-60° C. under vacuum until constant weight (2.07 g, 86.25% yield).

Workup

  1. additiontreated with aqueous 10%
  2. customat 45-55° C.
  3. customfor 3 hours
  4. custom30 minutes
  5. filtrationfiltered
  6. washThe cake was washed with deionised water (2×10 ml)
  7. customThe solid was dried at 50-60° C. under vacuum until constant weight (2.07 g, 86.25% yield)

Sources & evidence

ORD record
ord-d1b436780dad477da47bb00a7c78819e
Source dataset
uspto-grants-2012_03
Patent number
US08143397B2

Reaction notes

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