HCID 23111451, compound → HCID 23111436, compound
Reaction equation
COC1C=CC(N2CCN(CCC3C=CC=CC=3)CC2)=CC=1C.[F:24][C:25]1[CH:30]=[C:29]([O:31]C)[CH:28]=[CH:27][C:26]=1[N:33]1[CH2:38][CH2:37][N:36]([CH2:39][CH2:40][C:41]2[CH:46]=[CH:45][CH:44]=[CH:43][CH:42]=2)[CH2:35][CH2:34]1>>[F:24][C:25]1[CH:30]=[C:29]([OH:31])[CH:28]=[CH:27][C:26]=1[N:33]1[CH2:38][CH2:37][N:36]([CH2:39][CH2:40][C:41]2[CH:42]=[CH:43][CH:44]=[CH:45][CH:46]=2)[CH2:35][CH2:34]1Participants
3
Procedure
Production Example 10 was repeated except that 1-(4-methoxy-3-methylphenyl)-4-phenethylpiperazine was replaced with 1-(2-fluoro-4-methoxyphenyl)-4-phenethylpiperazine (367 mg), and the resulting crude product was purified on TLC (developer, chloroform: methanol=17:1) to provide 3-fluoro-4-(4-phenethyl-piperazin-1-yl)phenol (178 mg).
Workup
- customthe resulting crude product was purified on TLC (developer, chloroform: methanol=17:1)
Sources & evidence
- ORD record
- ord-a8646fb48410429faeb5da8ed5596706
- Source dataset
- uspto-grants-2008_11
- Patent number
- US07449466B2
Reaction notes
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