Lithium Hydroxide → HCID 67078536, compound

HRID 2105655Notes

Reaction equation

HRID 2105655 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

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

  1. customThe THF was removed on the rotovap
  2. extractionextracted with EtOAc
  3. washThe combined organics were washed with H2O, brine
  4. dry with materialdried (MgSO4)
  5. filtrationFiltration and evaporation
  6. 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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