Ethane, 2-bromo-1,1-diethoxy- → 6-Bromo-8-fluoroimidazo[1,2-a]pyridine
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([F:9])[C:5]([NH2:8])=[N:6][CH:7]=1.[CH2:10](OC(OCC)CBr)[CH3:11]>>[Br:1][C:2]1[CH:3]=[C:4]([F:9])[C:5]2[N:6]([CH:10]=[CH:11][N:8]=2)[CH:7]=1Participants
3
Procedure
Prepared from 5-bromo-3-fluoro-pyridin-2-ylamine (example C.29 step 3) (3.1 g, 15.7 mmol) and bromoacetaldehyde diethyl acetal (90%, 4.86 mL, 31.3 mmol) as described in example C.20 step 1. Obtained the title compound as a light brown solid (3.0 g, 89%). MS (ISP) 215.1 [(M+H)+], 217.1 [(M+2+H)+].
Sources & evidence
- ORD record
- ord-159bc7d4ff354a8baa7c91108cdb35b4
- Source dataset
- uspto-grants-2011_11
- Patent number
- US08063048B2
Reaction notes
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