Sulfuric Acid → HCID 19030761, compound
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]=1Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
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
- extractionextracted with chloroform
- dry with materialThe extract is dried with magnesium sulfate
- customthe solvent is evaporated off
- customThe resulting residue is purified by silica gel column chromatography (solvent: dichloromethane:methanol=50:1)
Sources & evidence
- ORD record
- ord-e1201d6d426140f2a3e1eee0ab041396
- Source dataset
- uspto-grants-1995_07
- Patent number
- US05436254
Reaction notes
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