Hydrogen Bromide → HCID 23001313, compound
Reaction equation
C[O:2][C:3]1[CH:4]=[C:5]([S:9]([CH2:12][CH2:13][CH2:14][N:15]2C(=O)C3C(=CC=CC=3)C2=O)(=[O:11])=[O:10])[CH:6]=[CH:7][CH:8]=1.[BrH:26]>C(O)(=O)C>[BrH:26].[NH2:15][CH2:14][CH2:13][CH2:12][S:9]([C:5]1[CH:4]=[C:3]([OH:2])[CH:8]=[CH:7][CH:6]=1)(=[O:10])=[O:11]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The sulfone from Step B (1.32 g, 3.67 mmol) in acetic acid (2 mL) and 48% HBr (2 mL) was heated at 100° C. for 72 hours. The reaction mixture was concentrated and the solid residue triturated with ether (200 mL) to produce the title compound as a grey solid.
Workup
- concentrationThe reaction mixture was concentrated
- customthe solid residue triturated with ether (200 mL)
Sources & evidence
- ORD record
- ord-6ca11fc85591452290b38b991ee8bf0f
- Source dataset
- uspto-grants-2003_08
- Patent number
- US06610722B2
Reaction notes
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