Water → HCID 86599808, compound

HRID 2374659Notes

Reaction equation

HRID 2374659 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-8afedd1d1717461382dd3e4130f0fd02
Source dataset
uspto-grants-2008_12
Patent number
US07462716B2

Reaction notes

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