2,2,2-Trifluoroethanol → HCID 66600081, compound
Reaction equation
[Br:1][C:2]1[C:3]([F:9])=[N:4][C:5]([CH3:8])=[CH:6][CH:7]=1.[F:10][C:11]([F:15])([F:14])[CH2:12][OH:13]>>[Br:1][C:2]1[C:3]([F:9])=[N:4][C:5]([CH2:8][O:13][CH2:12][C:11]([F:15])([F:14])[F:10])=[CH:6][CH:7]=1Participants
3
Procedure
The title compound was prepared in an analogous manner to that described in Example 198 (Step 1) using 3-bromo-2-fluoro-6-methylpyridine (1.44 g, 7.58 mmol) (Waterstone Technology) and 2,2,2-trifluoroethanol. 1H NMR (400 MHz, d6-DMSO) δ 8.34 (1H, t, J=8.5 Hz); 7.34 (1H, d, J=7.9 Hz); 4.69 (2 H, s); 4.22 (2 H, q, J=9.5 Hz). m/z (ESI, +ve ion) 288/290 (M+H)+.
Sources & evidence
- ORD record
- ord-b8b2e192394840e5832592c7204b063b
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08362241B2
Reaction notes
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