Lithium Hydroxide → HCID 67078536, compound
Reaction equation
C[O:2][C:3](=[O:39])[C@H:4]([NH:11][C:12]([C:14]12[CH2:21][C:18]([C:22]3[NH:30][C:29]4[C:28](=[O:31])[N:27]([CH2:32][CH2:33][CH3:34])[C:26](=[O:35])[N:25]([CH2:36][CH2:37][CH3:38])[C:24]=4[N:23]=3)([CH2:19][CH2:20]1)[CH2:17][CH2:16][CH2:15]2)=[O:13])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.[Li+].[OH-]>C1COCC1>[O:35]=[C:26]1[N:25]([CH2:36][CH2:37][CH3:38])[C:24]2[N:23]=[C:22]([C:18]34[CH2:21][C:14]([C:12]([NH:11][C@H:4]([C:5]5[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=5)[C:3]([OH:39])=[O:2])=[O:13])([CH2:20][CH2:19]3)[CH2:15][CH2:16][CH2:17]4)[NH:30][C:29]=2[C:28](=[O:31])[N:27]1[CH2:32][CH2:33][CH3:34]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of (1RS,2R,5SR)-{[5-(2,6-Dioxo-1,3-dipropyl-2,3,6,7-tetrahydro-1H-purin-8-yl)-bicyclo-[3.2.1]octane-1-carbonyl]-amino}-phenyl-acetic acid methyl ester (0.022 mmol, 0.012 g) in THF (2 ml) was treated with 1N LiOH (0.22 ml) for 3d. The THF was removed on the rotovap, the aqueous residue acidified (pH 2) with 1N HCl and extracted with EtOAc. The combined organics were washed with H2O, brine and dried (MgSO4). Filtration and evaporation followed by reverse phase HPLC purification provide the desired product (0.0055 g, 48%) as a mixture of diastereomers. HPLC (10% to 90% MeCN (0.1% TFA)/H2O (0.1% TFA), YMC 120 A/S-5 ODS-AM column, 100 mm×4.6 mm, 1.5 ml/min: RT=6.88 min.
Workup
- customThe THF was removed on the rotovap
- extractionextracted with EtOAc
- washThe combined organics were washed with H2O, brine
- dry with materialdried (MgSO4)
- filtrationFiltration and evaporation
- customfollowed by reverse phase HPLC purification
Sources & evidence
- ORD record
- ord-34990090a1fa46a5866798625596e1a4
- Source dataset
- uspto-grants-2009_08
- Patent number
- US07579354B2
Reaction notes
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