Hydrochloric Acid → HCID 22481224, compound
Reaction equation
[F:1][C:2]([F:25])([F:24])[C:3]1[CH:4]=[C:5]([C:9]2[C:14]([CH3:15])=[CH:13][C:12]([NH:16]C(=O)C(C)(C)C)=[C:11]([CH3:23])[CH:10]=2)[CH:6]=[CH:7][CH:8]=1.Cl.O>C(O)(=O)C>[F:1][C:2]([F:24])([F:25])[C:3]1[CH:4]=[C:5]([C:9]2[CH:10]=[C:11]([CH3:23])[C:12](=[CH:13][C:14]=2[CH3:15])[NH2:16])[CH:6]=[CH:7][CH:8]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 100 °C
Procedure
The product from stage b) (10.4 g) in glacial acetic acid (36 ml) was treated with hydrochloric acid (24.5 ml of 15% solution) at 70° C. The mixture was stirred for 3 days at 100° C. On cooling, water was added and the mixture extracted with ethyl acetate. The organic phase was washed with sodium bicarbonate solution, dried (MgSO4) and concentrated to give the title product.
Workup
- temperatureOn cooling
- extractionthe mixture extracted with ethyl acetate
- washThe organic phase was washed with sodium bicarbonate solution
- dry with materialdried (MgSO4)
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-7e2dfb6642f64a8190ec413c110413e4
- Source dataset
- uspto-grants-2005_05
- Patent number
- US06893650B1
Reaction notes
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