Reaction equation
[OH:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[C:5]([C:15]([O:17][CH2:18][CH3:19])=[O:16])[N:6]2[CH2:11][CH:12]([CH3:14])[CH3:13].S(C1C=CC([N+]([O-])=O)=CC=1)(O[CH2:24][C@H:25]1[O:27][CH2:26]1)(=O)=O.[CH:37]1[C:46]2[C:41](=[CH:42][CH:43]=[CH:44][CH:45]=2)[CH:40]=[CH:39][C:38]=1[CH:47]1[CH2:52][CH2:51][NH:50][CH2:49][CH2:48]1>>[OH:27][C@@H:25]([CH2:26][N:50]1[CH2:51][CH2:52][CH:47]([C:38]2[CH:39]=[CH:40][C:41]3[C:46](=[CH:45][CH:44]=[CH:43][CH:42]=3)[CH:37]=2)[CH2:48][CH2:49]1)[CH2:24][O:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[C:5]([C:15]([O:17][CH2:18][CH3:19])=[O:16])[N:6]2[CH2:11][CH:12]([CH3:14])[CH3:13]Participants
Reactant 3
Product 1
Procedure
By the reactions in the same manner as in Starting Material Synthesis Example 25 using ethyl 4-hydroxy-1-(2-methylpropyl)indole-2-carboxylate (5.0 g) obtained in Starting Material Synthesis Example 12, (S)-glycidyl nosylate (4.5 g) and 4-(naphthalen-2-yl)piperidine (5.3 g), ethyl (S)-4-(2-hydroxy-3-(4-(naphthalen-2-yl)piperidino)propyloxy)-1-(2-methylpropyl)indole-2-carboxylate (7.5 g) was obtained. This was dissolved in ethanol (40 ml) and water (30 ml) and potassium hydroxide (4.0 g) were added. The mixture was refluxed for 2.5 hr. From the obtained reaction mixture, ethanol was evaporated under reduced pressure and 1N aqueous hydrochloric acid solution (30 ml) was added under ice-cooling. The mixture was extracted with chloroform. The obtained organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and isopropyl ether was added to the obtained oil. The obtained crystals were collected by filtration to give the title compound (6.7 g) as pale-yellow crystals.
Workup
- customobtained
Sources & evidence
- ORD record
- ord-fce260f4538047b79c9d27d1079688cb
- Source dataset
- uspto-grants-2007_03
- Patent number
- US07196199B2
Linked notes
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