Hydrochloric Acid → HCID 136184229, compound
Reaction equation
C([O:8][C:9]1[C:14](=[O:15])[N:13]2[CH:16]=[C:17]([N:20]3[CH2:25][CH2:24][O:23][CH2:22][CH2:21]3)[CH:18]=[CH:19][C:12]2=[N:11][C:10]=1[C:26]1[N:30]=[C:29]([CH2:31][C:32]2[CH:37]=[CH:36][C:35]([F:38])=[CH:34][CH:33]=2)[O:28][N:27]=1)C1C=CC=CC=1.Cl>ClCCl>[F:38][C:35]1[CH:34]=[CH:33][C:32]([CH2:31][C:29]2[O:28][N:27]=[C:26]([C:10]3[N:11]=[C:12]4[CH:19]=[CH:18][C:17]([N:20]5[CH2:21][CH2:22][O:23][CH2:24][CH2:25]5)=[CH:16][N:13]4[C:14](=[O:15])[C:9]=3[OH:8])[N:30]=2)=[CH:37][CH:36]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of the product of example 22 (40 mg, 0.078 mmol) in dichloromethane (5 ml) was added FeCl3 (38 mg, 0.234 mmol), and the mixture was stirred at room temperature for 30 min. Then 1M HCl (8 ml) was added and the mixture was extracted with dichloromethane three times. The combined extracts were washed with water and brine, dried and evaporated into dryness. The residue was recrystallized from CH2Cl2/MeOH to give the titled products (10 mg, yield 30.3%).
Workup
- extractionthe mixture was extracted with dichloromethane three times
- washThe combined extracts were washed with water and brine
- customdried
- customevaporated into dryness
- customThe residue was recrystallized from CH2Cl2/MeOH
Sources & evidence
- ORD record
- ord-4d0051e970584a83b489937731bab701
- Source dataset
- uspto-grants-2013_10
- Patent number
- US08563562B2
Reaction notes
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