Methylamine → 3-{4-[(4-Fluorophenyl)methoxy]phenyl}-N-methylprop-2-enamide
Reaction equation
[F:1][C:2]1[CH:20]=[CH:19][C:5]([CH2:6][O:7][C:8]2[CH:13]=[CH:12][C:11]([CH:14]=[CH:15][C:16](O)=[O:17])=[CH:10][CH:9]=2)=[CH:4][CH:3]=1.[CH3:21][NH2:22]>>[F:1][C:2]1[CH:20]=[CH:19][C:5]([CH2:6][O:7][C:8]2[CH:13]=[CH:12][C:11]([CH:14]=[CH:15][C:16]([NH:22][CH3:21])=[O:17])=[CH:10][CH:9]=2)=[CH:4][CH:3]=1Participants
3
Procedure
The title compound is prepared in analogy to example 12 b) from 3-[4-(4-fluoro-benzyloxy)-phenyl]-acrylic acid and methylamine. Yield=21%. Colorless solid. MS: m/e=286.0 (M++H).
Sources & evidence
- ORD record
- ord-cb35523b78bd4be2ad4c83d9613ee1a8
- Source dataset
- uspto-grants-2005_05
- Patent number
- US06900354B2
Reaction notes
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