2-Methoxybenzaldehyde → 2-(2-methoxyphenyl)-3H-quinazolin-4-one
Reaction equation
[C:1]1([C:7]2[NH:16][C:15](=[O:17])[C:14]3[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=3)[N:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:18][O:19]C1C=CC=CC=1C=O>>[CH3:18][O:19][C:6]1[CH:5]=[CH:4][CH:3]=[CH:2][C:1]=1[C:7]1[NH:16][C:15](=[O:17])[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[N:8]=1Participants
3
Procedure
According to the preparation of 41, 2-methoxybenzaldehyde (33) (1.0 g, 7.3 mmol) was used to afford 42 (1.6 g, 89.1%) as pale yellow needles.
Sources & evidence
- ORD record
- ord-7af50da8f8964fd581bc48c4d25cb25d
- Source dataset
- uspto-grants-2002_11
- Patent number
- US06479499B1
Reaction notes
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