1-(Bromomethyl)-2,4-difluorobenzene → HCID 69507843, compound
Reaction equation
[CH2:1]([O:3][C:4]([C:6]1[CH:11]=[C:10]([C:12]2[CH2:16][CH2:15][CH2:14][C:13]=2[C:17]2[CH:22]=[C:21]([Cl:23])[CH:20]=[CH:19][C:18]=2[OH:24])[N:9]=[N:8][CH:7]=1)=[O:5])[CH3:2].[F:25][C:26]1[CH:33]=[C:32]([F:34])[CH:31]=[CH:30][C:27]=1[CH2:28]Br>>[CH2:1]([O:3][C:4]([C:6]1[CH:11]=[C:10]([C:12]2[CH2:16][CH2:15][CH2:14][C:13]=2[C:17]2[CH:22]=[C:21]([Cl:23])[CH:20]=[CH:19][C:18]=2[O:24][CH2:28][C:27]2[CH:30]=[CH:31][C:32]([F:34])=[CH:33][C:26]=2[F:25])[N:9]=[N:8][CH:7]=1)=[O:5])[CH3:2]Participants
3
Procedure
Prepared by general procedure F(iii) but using 6-{2-[5-chloro-2-(hydroxy)phenyl]cyclopent-1-enyl}-pyridazine-4-carboxylic acid ethyl ester instead of 6-{2-[5-methyl-2-(hydroxy)phenyl]cyclopent-1-enyl}pyridine-2-carboxylic acid ethyl ester and 2,4-difluorobenzyl bromide instead of 4-fluorobenzyl bromide.
Workup
- customPrepared by general procedure F(iii)
Sources & evidence
- ORD record
- ord-b5fb82cd7fb44d0ebf443589826ae3c0
- Source dataset
- uspto-grants-2007_06
- Patent number
- US07232821B2
Reaction notes
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