3-Fluorobenzaldehyde → HCID 59753870, compound
Reaction equation
Br[C:2]1[C:3]([Cl:9])=[N:4][C:5]([Cl:8])=[N:6][CH:7]=1.[F:10][C:11]1[CH:12]=[C:13]([CH:16]=[CH:17][CH:18]=1)[CH:14]=[O:15]>>[Cl:8][C:5]1[N:4]=[C:3]([Cl:9])[C:2]([CH:14]([C:13]2[CH:16]=[CH:17][CH:18]=[C:11]([F:10])[CH:12]=2)[OH:15])=[CH:7][N:6]=1Participants
3
Procedure
The compound was prepared from 5-bromo-2,4-dichloropyrimidine (Aldrich) and 3-fluorobenzaldehyde (Aldrich) in 79% yield in an analogous manner as described in Example 1. 1H NMR (300 MHz, CDCl3) δ 8.85 (s, 1H), 7.35 (m, 1H), 7.14 (m, 3H), 7.14 (m, 3H), 6.077 (s, 1H).
Sources & evidence
- ORD record
- ord-c174a9d949804ab9a9788be11e3ab0fe
- Source dataset
- uspto-grants-2008_07
- Patent number
- US07405220B2
Reaction notes
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