1,2-Dibromoethane → 4-Iodopyrazole
Reaction equation
[I:1][C:2]1[CH:3]=[N:4][NH:5][CH:6]=1.Br[CH2:8][CH2:9][Cl:10].BrCCBr>C1(C)C=CC=CC=1>[I:1][C:2]1[CH:3]=[N:4][N:5]([CH2:8][CH2:9][Cl:10])[CH:6]=1.[I:1][C:2]1[CH:3]=[N:4][NH:5][CH:6]=1Participants
6
Reactant 3
Product 2
Reagents, catalysts & solvents 1
Procedure
When an equivalent amount of 4-iodopyrazole is substituted for 1-ethoxycarbonyl-2H-indazolin-3-one and 2-bromochloroethane is substituted for 1,2-dibromoethane in the procedure of Example 19 using toluene as solvent, 2-(4-iodo-1H-pyrazol-1-yl)ethyl chloride is isolated after column chromatography (4-iodopyrazole, Aldrich, 41%, C).
Sources & evidence
- ORD record
- ord-9a53361bc42c43f8b6c1b6aea62a9bb8
- Source dataset
- uspto-grants-1991_10
- Patent number
- US05053411
Reaction notes
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