3-Bromo-6-chloro-2-methylpyridine → 3-Bromo-2-(bromomethyl)-6-chloropyridine
Reaction equation
[Br:1][C:2]1[C:3]([CH3:9])=[N:4][C:5]([Cl:8])=[CH:6][CH:7]=1.[Br:10]C1C(CBr)=NC=C(Br)C=1>>[Br:1][C:2]1[C:3]([CH2:9][Br:10])=[N:4][C:5]([Cl:8])=[CH:6][CH:7]=1Participants
3
Procedure
Compound 55B (0.33 g, 45%) was prepared from 55A (0.53 g, 2.57 mmol) using a procedure similar to the synthesis of 52B. HPLC Rt=2.47 min.
Sources & evidence
- ORD record
- ord-e81759140f404bed8febb149f307e60d
- Source dataset
- uspto-grants-2008_05
- Patent number
- US07378426B2
Reaction notes
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