Methanol → HCID 59571743, compound
Reaction equation
[OH-].[Na+:2].O1CCCC1.CO.[CH3:10][C:11]1[O:15][C:14]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[N:13][C:12]=1[CH2:22][O:23][C:24]1[CH:56]=[CH:55][C:27]([CH2:28][N:29]2[C:41]3[CH:40]=[CH:39][CH:38]=[CH:37][C:36]=3[C:35]3[C:30]2=[CH:31][CH:32]=[CH:33][C:34]=3[O:42][CH2:43][C:44]2[CH:54]=[CH:53][C:47]([C:48]([O:50]CC)=[O:49])=[CH:46][CH:45]=2)=[CH:26][C:25]=1[O:57][CH3:58]>O>[CH3:10][C:11]1[O:15][C:14]([C:16]2[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=2)=[N:13][C:12]=1[CH2:22][O:23][C:24]1[CH:56]=[CH:55][C:27]([CH2:28][N:29]2[C:41]3[CH:40]=[CH:39][CH:38]=[CH:37][C:36]=3[C:35]3[C:30]2=[CH:31][CH:32]=[CH:33][C:34]=3[O:42][CH2:43][C:44]2[CH:45]=[CH:46][C:47]([C:48]([O-:50])=[O:49])=[CH:53][CH:54]=2)=[CH:26][C:25]=1[O:57][CH3:58].[Na+:2]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
1 mL of 5 N sodium hydroxide solution was added to tetrahydrofuran:methanol=1:1(20 mL) solution of 110 mg of ethyl 4-((9-(4-((5-methyl-2-phenyloxazole-4-yl)methoxy)-3-methoxybenzyl)-9H-carbazole-5-yloxy)methyl)benzoate, and stirred at 70° C. for 1 hour. The reaction mixture was allowed to cool, and the water was added thereto. The crystalline precipitate was isolated by filtration, and washed with 2-propanol. The collected precipitate was dried under reduced pressure, and 107 mg of the subject compound was prepared as white crystal.
Workup
- temperatureto cool
- customThe crystalline precipitate was isolated by filtration
- washwashed with 2-propanol
- dry with materialThe collected precipitate was dried under reduced pressure, and 107 mg of the subject compound
- customwas prepared as white crystal
Sources & evidence
- ORD record
- ord-3c12c8d1faa24d5aa6ce0c2f7974d237
- Source dataset
- uspto-grants-2012_12
- Patent number
- US08329913B2
Reaction notes
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