Hydrochloric Acid → HCID 66668301, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4](/[CH:9]=[CH:10]/[C:11]([C:13]2[CH:14]=[N:15][C:16]([O:19]C)=[CH:17][CH:18]=2)=[O:12])[CH:5]=[C:6]([Cl:8])[CH:7]=1.Cl>O1CCOCC1>[Cl:8][C:6]1[CH:5]=[C:4](/[CH:9]=[CH:10]/[C:11]([C:13]2[CH:18]=[CH:17][C:16](=[O:19])[NH:15][CH:14]=2)=[O:12])[CH:3]=[C:2]([Cl:1])[CH:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In analogy to example 162, step 2, (E)-3-(3,5-dichlorophenyl)-1-(6-methoxypyridin-3-yl)prop-2-en-1-one was reacted with concentrated aqueous HCl in 1,4-dioxane to give the title compound as a colourless solid.
Sources & evidence
- ORD record
- ord-d70e9eb35e2745bf981ee78b1d928a5a
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08765730B2
Reaction notes
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