Acetone → sodium;(E)-7-[3-(4-fluorophenyl)-1-propan-2-ylindol-2-yl]-3,5-dihydroxyhept-6-enoate

HRID 2219851Notes

Reaction equation

HRID 2219851 reaction equation
[CH3:1][CH:2]([N:4]1[C:12](/[CH:13]=[CH:14]/[C@H:15]([OH:24])[CH2:16][C@H:17]([OH:23])[CH2:18][C:19]([O:21]C)=[O:20])=[C:11]([C:25]2[CH:30]=[CH:29][C:28]([F:31])=[CH:27][CH:26]=2)[C:10]2[C:5]1=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH3:3].[OH-].[Na+:33].CC(C)=O>CO>[CH3:3][CH:2]([N:4]1[C:12](/[CH:13]=[CH:14]/[CH:15]([OH:24])[CH2:16][CH:17]([OH:23])[CH2:18][C:19]([O-:21])=[O:20])=[C:11]([C:25]2[CH:26]=[CH:27][C:28]([F:31])=[CH:29][CH:30]=2)[C:10]2[CH:9]=[CH:8][CH:7]=[CH:6][C:5]1=2)[CH3:1].[Na+:33]

Participants

5

Reactant 3

HCID 180AcetoneHCID 14798Sodium HydroxideHCID 13741557Fluvastatin methyl ester

Product 1

HCID 16760425sodium;(E)-7-[3-(4-fluorophenyl)-1-propan-2-ylindol-2-yl]-3,5-dihydroxyhept-6-enoateYield 43.8%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

Fluvastatin methyl ester (3.0 g) was dissolved in MeOH (15 ml) by heating to reflux. NaOH (0.29 g) was added and the clear solution was stirred at reflux for 30 min, then acetone (75 ml) was added. The solution was cooled to room temperature and stirred over night. The product was isolated by filtration under nitrogen, washed with acetone (35 ml) and dried at 50° C. in a vacuum oven for 21.5 h to obtain 1.34 g of fluvastatin sodium crystal Form LXV.

Workup

  1. temperatureby heating to reflux
  2. temperatureat reflux for 30 min
  3. stirringstirred over night
  4. customThe product was isolated by filtration under nitrogen
  5. washwashed with acetone (35 ml)
  6. customdried at 50° C. in a vacuum oven for 21.5 h

Sources & evidence

ORD record
ord-603f757b0c614ea389e7f976592bc23c
Source dataset
uspto-grants-2008_08
Patent number
US07414140B2

Reaction notes

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