Water → HCID 12132661, compound
Reaction equation
C([O:4][CH2:5][C:6]1[C:32]([F:33])=[C:31]([NH2:34])[C:9]2[C:10](=[O:30])[CH:11]=[C:12]([C:14]3[CH:19]=[CH:18][C:17]([NH:20][C:21](=[O:28])[CH2:22][CH2:23][CH2:24][N:25]([CH3:27])[CH3:26])=[C:16]([F:29])[CH:15]=3)[O:13][C:8]=2[C:7]=1[F:35])(=O)C.[OH-].[Na+].O>CO>[NH2:34][C:31]1[C:9]2[C:10](=[O:30])[CH:11]=[C:12]([C:14]3[CH:19]=[CH:18][C:17]([NH:20][C:21](=[O:28])[CH2:22][CH2:23][CH2:24][N:25]([CH3:26])[CH3:27])=[C:16]([F:29])[CH:15]=3)[O:13][C:8]=2[C:7]([F:35])=[C:6]([CH2:5][OH:4])[C:32]=1[F:33]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a suspension of 1j (363 mg, 0.739 mmol) in methanol (36 mL) was added 1 mol/L sodium hydroxide (4 mL), and the mixture was stirred at room temperature for 20 minutes. Water was added thereto and the crystals precipitated were collected by filtration. Purification by silica gel column chromatography gave a free base of 1k (299 mg, 69%), which was converted into a hydrochloride.
Workup
- customthe crystals precipitated
- filtrationwere collected by filtration
- customPurification by silica gel column chromatography
Sources & evidence
- ORD record
- ord-c3ca9120d3774776a54b514c08cdb244
- Source dataset
- uspto-grants-2004_11
- Patent number
- US06812246B2
Reaction notes
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