(2-Chloropyridin-3-yl)methanol → 3-(Bromomethyl)-2-chloropyridine
Reaction equation
ClC1C(CO)=CC=CN=1.[Br:10][CH2:11][C:12]1[C:13]([Cl:20])=[N:14][C:15](Cl)=[C:16](F)[CH:17]=1>>[Br:10][CH2:11][C:12]1[C:13]([Cl:20])=[N:14][CH:15]=[CH:16][CH:17]=1Participants
3
Procedure
Compound 12B (0.22 g, 78%) was prepared from 12A (0.20 g, 1.39 mmol) using a procedure similar to the synthesis of 1B. HPLC Rt=1.94 min.
Sources & evidence
- ORD record
- ord-14a4f5c969c4475ebf6f1875d117b296
- Source dataset
- uspto-grants-2008_05
- Patent number
- US07378426B2
Reaction notes
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