Sodium Hydroxide → HCID 18475415, compound
Reaction equation
C([O:3][C:4](=[O:31])[CH:5]([C:24]1[CH:25]=[N:26][C:27]([CH3:30])=[N:28][CH:29]=1)[CH2:6][CH2:7][C:8](=[O:23])[CH2:9][CH2:10][CH2:11][CH2:12][C:13]1[CH:22]=[CH:21][C:20]2[CH2:19][CH2:18][CH2:17][NH:16][C:15]=2[N:14]=1)C.[OH-].[Na+]>C(O)C>[CH3:30][C:27]1[N:28]=[CH:29][C:24]([CH:5]([CH2:6][CH2:7][C:8](=[O:23])[CH2:9][CH2:10][CH2:11][CH2:12][C:13]2[CH:22]=[CH:21][C:20]3[CH2:19][CH2:18][CH2:17][NH:16][C:15]=3[N:14]=2)[C:4]([OH:31])=[O:3])=[CH:25][N:26]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 1-10a (0.15 g, 0.353 mmol) in ethanol (1 mL) was added NaOH (0.39 rnL of 1N solution in water, 0.39 mmol). After 30 minutes, the mixture was concentrated, and the residue chromatographed on silica gel (20:10:1:1 to 10:10:1:1 ethyl acetate/ethanol/NH4OH/water) to give 1-11a as a white solid.
Workup
- concentrationthe mixture was concentrated
- customthe residue chromatographed on silica gel (20:10:1:1 to 10:10:1:1 ethyl acetate/ethanol/NH4OH/water)
Sources & evidence
- ORD record
- ord-c36a6779ef9d414097586960c3d788ca
- Source dataset
- uspto-grants-2002_06
- Patent number
- US06410526B1
Reaction notes
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