Phosphorus tribromide → HCID 59589453, compound
Reaction equation
[Cl:1][C:2]1[N:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]2=[N:4][C:3]=1[CH2:11]O.[Br:13]P(Br)Br>C(Cl)(Cl)Cl>[Br:13][CH2:11][C:3]1[N:4]=[C:5]2[CH:10]=[CH:9][CH:8]=[CH:7][N:6]2[C:2]=1[Cl:1]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of {3-chloroimidazo[1,2-a]pyridin-2-yl}methanol (0.799 g, 4.39 mmol) in anhydrous chloroform (25 mL) at 0° C. was added tribromophosphane (1.20 g, 0.41 mL, 4.43 mmol), and the reaction mixture was allowed to stir at room temperature overnight. The solvent was evaporated to provide the crude 2-(bromomethyl)-3-chloroimidazo[1,2-a]pyridine, which was used for the next step without any further purification; M+1 246.2.
Workup
- customThe solvent was evaporated
Sources & evidence
- ORD record
- ord-ddcdea4451c1481ebadbe6af1592b18d
- Source dataset
- uspto-grants-2015_05
- Patent number
- US09040538B2
Reaction notes
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