4-Fluorostyrene → HCID 68435316, compound
Reaction equation
Br[C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][C:6](Cl)=[N:7]2.[CH3:13][C:14]1[O:18][C:17]([CH2:19][NH2:20])=[CH:16][CH:15]=1.[F:21][C:22]1[CH:29]=[CH:28][C:25]([CH:26]=[CH2:27])=[CH:24][CH:23]=1>>[F:21][C:22]1[CH:29]=[CH:28][C:25](/[CH:26]=[CH:27]/[C:2]2[CH:11]=[CH:10][CH:9]=[C:8]3[C:3]=2[CH:4]=[CH:5][C:6]([NH:20][CH2:19][C:17]2[O:18][C:14]([CH3:13])=[CH:15][CH:16]=2)=[N:7]3)=[CH:24][CH:23]=1Participants
4
Procedure
The title compound, MS: m/e=359.0 (M+H+), was prepared in accordance with the general method of example 2 from 5-bromo-2-chloroquinoline, 5-methyl-2-furanmethanamine and 4-fluorostyrene.
Sources & evidence
- ORD record
- ord-840fb810e5854f12b4cce2d254fff84e
- Source dataset
- uspto-grants-2010_11
- Patent number
- US07825253B2
Reaction notes
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