4-Fluorobenzaldehyde → HCID 22675140, compound
Reaction equation
[CH3:1][N:2]([CH2:16][CH2:17][OH:18])[C:3]1[N:8]=[CH:7][CH:6]=[C:5]([C:9]2[CH:15]=[CH:14][C:12]([NH2:13])=[CH:11][CH:10]=2)[N:4]=1.F[C:20]1[CH:27]=[CH:26][C:23]([CH:24]=[O:25])=[CH:22][CH:21]=1>>[CH3:1][N:2]([CH2:16][CH2:17][O:18][C:20]1[CH:27]=[CH:26][C:23]([CH:24]=[O:25])=[CH:22][CH:21]=1)[C:3]1[N:8]=[CH:7][CH:6]=[C:5]([C:9]2[CH:15]=[CH:14][C:12]([NH2:13])=[CH:11][CH:10]=2)[N:4]=1Participants
3
Procedure
The title compound (980 mg) was prepared by the same procedure as the preparation 3 except for using 2-[N-methyl-N-(6-(4-anilinyl)pyrimidinyl)amino]ethanol (1.34 g) and 4-fluorobenzaldehyde (1.13 g).
Sources & evidence
- ORD record
- ord-6f64a764a15c45f1be176b4642497d0c
- Source dataset
- uspto-grants-2004_09
- Patent number
- US06787551B2
Reaction notes
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