HCID 11431603, compound → HCID 69316333, compound
Reaction equation
[Br:1][C:2]1[CH:7]=[C:6]([CH:8]([CH3:10])[CH3:9])[CH:5]=[CH:4][C:3]=1[C:11]1[CH:12]=[C:13]2[N:21]3[C:16](=[CH:17][C:18]([CH3:22])=[N:19][C:20]=13)[N:15]([CH:23]([CH2:27][CH2:28][CH3:29])[CH2:24][CH2:25][CH3:26])[C:14]2=[N:30][CH3:31].[ClH:32].C(OCC)(=O)C>C(OCC)(=O)C.C(O)C>[ClH:32].[Br:1][C:2]1[CH:7]=[C:6]([CH:8]([CH3:9])[CH3:10])[CH:5]=[CH:4][C:3]=1[C:11]1[CH:12]=[C:13]2[N:21]3[C:16](=[CH:17][C:18]([CH3:22])=[N:19][C:20]=13)[N:15]([CH:23]([CH2:27][CH2:28][CH3:29])[CH2:24][CH2:25][CH3:26])[C:14]2=[N:30][CH3:31]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a suspension of [4-(2-bromo-4-isopropyl-phenyl)-6-methyl-1-(1-propyl-butyl)-1H-1,5,7b-triaza-cyclopenta[cd]inden-2-ylidene]-methyl-amine (135 mg) in a mixture of ethyl acetate (1.5 mL) and ethanol (0.2 mL) was added 4M HCl/ethyl acetate (0.25 mL) and concentrated under reduced pressure. The residue was solidified from Et2O to provide the title compound as an amorphous (73 mg).
Workup
- concentrationconcentrated under reduced pressure
Sources & evidence
- ORD record
- ord-5242085275ae4c6c8a16192906bf8391
- Source dataset
- uspto-grants-2008_04
- Patent number
- US07365078B2
Reaction notes
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