3-Methoxybenzaldehyde → 2-(3-methoxyphenyl)quinazolin-4(3H)-one
Reaction equation
CO[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[C:9]1[NH:18][C:17](=[O:19])[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[N:10]=1.[CH3:20][O:21]C1C=C(C=CC=1)C=O>>[CH3:20][O:21][C:6]1[CH:5]=[C:4]([C:9]2[NH:18][C:17](=[O:19])[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[N:10]=2)[CH:3]=[CH:8][CH:7]=1Participants
3
Procedure
According to the preparation of 42, 3-methoxybenzaldehyde (34) (1.0 g, 7.3 mmol) was used to afford 43 (1.7 g, 95.0%) as pale yellow needles.
Sources & evidence
- ORD record
- ord-d7521595276c44efba1b8769455b49e7
- Source dataset
- uspto-grants-2002_11
- Patent number
- US06479499B1
Reaction notes
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