Hydrogen chloride-ethyl acetate → HCID 178478872, compound
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[C:12]3[CH:13]=[C:14]([C:17]4[C:18]([C:22]5[CH:27]=[CH:26][C:25]([F:28])=[CH:24][CH:23]=5)=[N:19][NH:20][CH:21]=4)[CH:15]=[CH:16][C:11]=3[N:10]=[C:9]2[O:29]C)=[CH:4][CH:3]=1.[ClH:31].C(OCC)(=O)C>CO>[ClH:31].[ClH:31].[F:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[C:12]3[CH:13]=[C:14]([C:17]4[C:18]([C:22]5[CH:27]=[CH:26][C:25]([F:28])=[CH:24][CH:23]=5)=[N:19][NH:20][CH:21]=4)[CH:15]=[CH:16][C:11]=3[N:10]=[C:9]2[OH:29])=[CH:4][CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
15 mg 1-(4-fluorophenyl)-6-[3-(4-fluorophenyl)-1H-4-pyrazolyl]-2-methoxy-1H-benzo [d] imidazole obtained in Example 139 was dissolved in methanol, then 2 mL of 4 N hydrochloric acid/ethyl acetate was added thereto, and the solvent was evaporated. The residue was crystallized from methanol/ether and then washed with ethyl acetate to give 12 mg of the title compound as colorless crystals.
Workup
- customthe solvent was evaporated
- customThe residue was crystallized from methanol/ether
- washwashed with ethyl acetate
Sources & evidence
- ORD record
- ord-f2facef0fc7d47cfa2f2bb2ba67f9cbb
- Source dataset
- uspto-grants-2006_07
- Patent number
- US07074801B1
Reaction notes
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