Lithium Hydroxide → HCID 86698149, compound
Reaction equation
C([O:7][CH2:8][CH2:9][CH2:10][CH2:11][N:12]1[C:20]2[C:15](=[N:16][C:17]([Cl:21])=[CH:18][CH:19]=2)[N:14]=[C:13]1[CH2:22][N:23]1[C:27]2[CH:28]=[N:29][CH:30]=[CH:31][C:26]=2[N:25]([CH:32]2[CH2:34][CH2:33]2)[C:24]1=[O:35])(=O)C(C)(C)C.[OH-].[Li+]>C1COCC1.O>[Cl:21][C:17]1[N:16]=[C:15]2[N:14]=[C:13]([CH2:22][N:23]3[C:27]4[CH:28]=[N:29][CH:30]=[CH:31][C:26]=4[N:25]([CH:32]4[CH2:34][CH2:33]4)[C:24]3=[O:35])[N:12]([CH2:11][CH2:10][CH2:9][CH2:8][OH:7])[C:20]2=[CH:19][CH:18]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
Compound 3 (0.29 g, 0.58 mmol) was dissolved in THF (15 mL) and lithium hydroxide (40 mg, 1.6 mmol) dissolved in water (5 mL) was added. The resulting mixture was stirred at room temperature overnight. The reaction mixture was poured in water and extracted with ethyl acetate. The organic layer was dried over MgSO4 and concentrated. The residue was purified by column chromatography using dichloromethane and methanol. The title compound 14 was isolated as a white powder (200 mg, 80%). m/z=414 (M+H)+.
Workup
- additionwas added
- extractionextracted with ethyl acetate
- dry with materialThe organic layer was dried over MgSO4
- concentrationconcentrated
- customThe residue was purified by column chromatography
Sources & evidence
- ORD record
- ord-fd49e03d2ab747baa9e49b05876c14f5
- Source dataset
- uspto-grants-2015_01
- Patent number
- US08927720B2
Reaction notes
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