Sulfuric Acid → HCID 19030761, compound

HRID 266835Notes

Reaction equation

HRID 266835 reaction equation
[O:1]1C[CH:2]1[CH2:4][CH2:5][CH2:6][CH2:7][O:8][C:9]1[CH:33]=[CH:32][C:12]([C:13]([N:15]2[CH2:20][CH2:19][CH:18]([N:21]3[C:31]4[C:26](=[CH:27][CH:28]=[CH:29][CH:30]=4)[CH2:25][CH2:24][C:22]3=[O:23])[CH2:17][CH2:16]2)=[O:14])=[CH:11][CH:10]=1.S(=O)(=O)(O)O.[C:39](=[O:42])([O-])O.[Na+]>O1CCOCC1.O>[OH:1][CH:2]([CH2:39][OH:42])[CH2:4][CH2:5][CH2:6][CH2:7][O:8][C:9]1[CH:10]=[CH:11][C:12]([C:13]([N:15]2[CH2:16][CH2:17][CH:18]([N:21]3[C:31]4[C:26](=[CH:27][CH:28]=[CH:29][CH:30]=4)[CH2:25][CH2:24][C:22]3=[O:23])[CH2:19][CH2:20]2)=[O:14])=[CH:32][CH:33]=1

Participants

6

Procedure

1-{1-[4-(4-Oxiranylbutoxy)benzoyl]-4-piperidinyl}-3,4-dihydrocarbostyril (1.6 g) is dissolved in a mixture of dioxane (30 ml) and water (10 ml). Thereto is added conc. sulfuric acid (0.1 ml) and the mixture is stirred at room temperature overnight. The mixture is neutralized with sodium hydrogen carbonate and then extracted with chloroform. The extract is dried with magnesium sulfate and the solvent is evaporated off. The resulting residue is purified by silica gel column chromatography (solvent: dichloromethane:methanol=50:1) to give 1-{1-[4-(5,6-dihydroxyhexyloxy)benzoyl]-4-piperidinyl}-3,4-dihydrocarbostyril (0.6 g).

Workup

  1. extractionextracted with chloroform
  2. dry with materialThe extract is dried with magnesium sulfate
  3. customthe solvent is evaporated off
  4. customThe resulting residue is purified by silica gel column chromatography (solvent: dichloromethane:methanol=50:1)

Sources & evidence

ORD record
ord-04116d50944f41ef98102e90687f3a6c
Source dataset
uspto-grants-1997_07
Patent number
US05652247

Reaction notes

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