Water → HCID 57846996, compound
Reaction equation
[NH:1]1[CH:5]=[CH:4][N:3]=[C:2]1[C@H:6]1[C@H:15]2[CH2:16][CH2:17][N:18]([C:19]([C@H:21]3[CH2:26][CH2:25][CH2:24][CH2:23][C@H:22]3[NH:27][C:28](=[O:35])[C:29]3[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=3)=[O:20])[C@H:14]2[C:13]2[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=2[NH:7]1.[H-].[Na+].[CH3:38]I.O>CN(C=O)C>[CH3:38][N:1]1[CH:5]=[CH:4][N:3]=[C:2]1[C@H:6]1[C@H:15]2[CH2:16][CH2:17][N:18]([C:19]([C@H:21]3[CH2:26][CH2:25][CH2:24][CH2:23][C@H:22]3[NH:27][C:28](=[O:35])[C:29]3[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=3)=[O:20])[C@H:14]2[C:13]2[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=2[NH:7]1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of the compound (119 mg, 0.252 mmol) synthesized in Example 81 in DMF (1 ml) was added sodium hydride (60% in oil, 12.1 mg, 0.30 mmol) under ice-cooling, and the mixture was stirred for 1 hr. Methyl iodide (0.0187 ml, 0.30 mmol) was added dropwise and the mixture was stirred overnight at room temperature. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous MgSO4, and the solvent was evaporated under reduced pressure. The residue was subjected to column chromatography using silica gel and eluted with hexane-ethyl acetate (5:95, v/v) to give the title compound (76.5 mg, 63%) as an amorphous form.
Workup
- temperaturecooling
- stirringthe mixture was stirred overnight at room temperature
- extractionthe mixture was extracted with ethyl acetate
- dry with materialThe extract was dried over anhydrous MgSO4
- customthe solvent was evaporated under reduced pressure
- washeluted with hexane-ethyl acetate (5:95
Sources & evidence
- ORD record
- ord-43263ccab9d243a5b93727d827321156
- Source dataset
- uspto-grants-2009_09
- Patent number
- US07592453B2
Reaction notes
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