Lithium Hydroxide → HCID 53373031, compound
Reaction equation
[Li+].[OH-].CC1C(C([O:11][CH2:12][C:13]2[CH:18]=[CH:17][C:16]([C:19]34[N:37]([C:38]([C:40]5[C:41]([CH3:45])=[N:42][O:43][CH:44]=5)=[O:39])[CH2:36][CH2:35][N:20]3[C:21](=[O:34])[C:22]3[N:23]([CH:25]=[C:26]([C:28]5[CH:29]=[N:30][CH:31]=[CH:32][CH:33]=5)[CH:27]=3)[CH2:24]4)=[CH:15][CH:14]=2)=O)=CON=1.CO.CC#N>[Cl-].[Na+].O>[OH:11][CH2:12][C:13]1[CH:18]=[CH:17][C:16]([C:19]23[N:37]([C:38]([C:40]4[C:41]([CH3:45])=[N:42][O:43][CH:44]=4)=[O:39])[CH2:36][CH2:35][N:20]2[C:21](=[O:34])[C:22]2[N:23]([CH:25]=[C:26]([C:28]4[CH:29]=[N:30][CH:31]=[CH:32][CH:33]=4)[CH:27]=2)[CH2:24]3)=[CH:15][CH:14]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Aqueous LiOH solution (1M)(0.75 mg, 0.018 mmol) was added to a solution of 4-{1-[(3-methyl-1,2-oxazol-4-yl)carbonyl]-5-oxo-7-(pyridin-3-yl)-2,3-dihydro-1H,5H-imidazo[1,2-a]pyrrolo[1,2-d]pyrazin-10a(10H)-yl}benzyl 3-methyl-1,2-oxazole-4-carboxylate (9.6 mg, 0.016 mmol) in a mixture MeOH/CH3CN (2 mL) and stirred at room temperature for 3 h. Brine (1 mL) was added and the resultant mixture was extracted with EtOAc (3×1 mL). The organic layers were combined, dried (MgSO4) and concentrated in vacuo to give a residue that was purified by flash chromatography (Biotage SP4 gradient 0-10% MeOH in EtOAc, 10 CV and hold 10 CV). The compound 10a-[4-(hydroxymethyl)phenyl]-1-[(3-methyl-1,2-oxazol-4-yl)carbonyl]-7-(pyridin-3-yl)-2,3,10,10a-tetrahydro-1H,5H-imidazo[1,2-a]pyrrolo[1,2-d]pyrazin-5-one (95) was isolated as a white solid (2.8 mg, yield 37%).
Workup
- extractionthe resultant mixture was extracted with EtOAc (3×1 mL)
- dry with materialdried (MgSO4)
- concentrationconcentrated in vacuo
- customto give a residue that
- customwas purified by flash chromatography (Biotage SP4 gradient 0-10% MeOH in EtOAc, 10 CV and hold 10 CV)
Sources & evidence
- ORD record
- ord-c195e01fc75a48d6b71b1fc6666c4ffa
- Source dataset
- uspto-grants-2013_12
- Patent number
- US08604034B2
Reaction notes
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