2-Bromo-6-(bromomethyl)pyridine → 2-{2-[(6-Bromopyridin-2-yl)methyoxy]ethyl}-2-azaspiro[3.3]heptane
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH2:8]Br)[N:3]=1.[CH2:10]1[C:13]2([CH2:16][CH2:15][CH2:14]2)[CH2:12][N:11]1[CH2:17][CH2:18][OH:19]>>[Br:1][C:2]1[N:3]=[C:4]([CH2:8][O:19][CH2:18][CH2:17][N:11]2[CH2:12][C:13]3([CH2:16][CH2:15][CH2:14]3)[CH2:10]2)[CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
The title compound was prepared according to Example 251, Step 1 using 2-bromo-6-(bromomethyl)pyridine (Example 190, Step 1) (200 mg, 0.80 mmol) and 2-(2-azaspiro[3.3]hept-2-yl)ethanol (112 mg, 0.80 mmol) as the starting materials.
Sources & evidence
- ORD record
- ord-e272ac40106e45f18ccecd8f8c636756
- Source dataset
- uspto-grants-2013_02
- Patent number
- US08367706B2
Reaction notes
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