Water → HCID 86599808, compound

HRID 1593727Notes

Reaction equation

HRID 1593727 reaction equation
[CH3:1][CH2:2][C@@H:3]([C:5]([O:7][C@@H:8]1[C@@H:13]2[C@@H:14]([CH2:19][CH2:20][C@@H:21]([OH:29])[CH2:22][C@@H:23]([OH:28])[CH2:24][C:25]([O-:27])=[O:26])[C@@H:15]([CH3:18])[CH:16]=[CH:17][C:12]2=[CH:11][C@@H:10]([OH:30])[CH2:9]1)=[O:6])[CH3:4].[Na+].[Br:32][CH2:33][CH2:34][CH2:35][CH2:36]Br.O.C(OCC)C>CN(C)C=O>[Br:32][CH2:33][CH2:34][CH2:35][CH2:36][O:26][C:25](=[O:27])[CH2:24][CH:23]([OH:28])[CH2:22][CH:21]([OH:29])[CH2:20][CH2:19][CH:14]1[CH:13]2[C:12](=[CH:11][CH:10]([OH:30])[CH2:9][CH:8]2[O:7][C:5](=[O:6])[CH:3]([CH3:4])[CH2:2][CH3:1])[CH:17]=[CH:16][CH:15]1[CH3:18]

Participants

6

Procedure

To a solution of pravastatin sodium (9.25 g, 21 mmol) in N,N-dimethylformamide (70 ml) a mixture of 1,4-dibromobutane (3.68 ml, 31 mmol) in N,N-dimethylformamide (30 ml) was added dropwise. The reaction mixture was stirred at room temperature for 24 h. The solution was then treated with water and diethyl ether, the organic layers were dried with sodium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography, with n-hexane/ethyl acetate 3/7 as eluent. The title compound was obtained as a white powder (7.8 g).

Workup

  1. additionwas added dropwise
  2. dry with materialthe organic layers were dried with sodium sulfate
  3. concentrationconcentrated under reduced pressure
  4. customThe residue was purified by flash chromatography, with n-hexane/ethyl acetate 3/7 as eluent

Sources & evidence

ORD record
ord-5ea111b3ac714188ae0a4a7565ee04d3
Source dataset
uspto-grants-2007_11
Patent number
US07297808B2

Reaction notes

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