p-Bromochlorobenzene → (3R)-1-(4-chlorophenyl)-3-methylpiperazine
Reaction equation
FC1C=CC([C:8]2[CH:13]=[CH:12][C:11]([N:14]3[CH2:19][CH2:18][NH:17][C@H:16]([CH3:20])[CH2:15]3)=[CH:10][CH:9]=2)=CC=1.BrC1C=CC([Cl:28])=CC=1>>[Cl:28][C:8]1[CH:13]=[CH:12][C:11]([N:14]2[CH2:19][CH2:18][NH:17][C@H:16]([CH3:20])[CH2:15]2)=[CH:10][CH:9]=1Participants
3
Procedure
The title compound was prepared following the procedure of Intermediate 22 but starting from 1-bromo-4-chlorobenzene. Purification by flash chromatography (CHCl3/MeOH) gave the title compound as a beige solid. M+(ESI): 211.2. HPLC purity: >96%).
Workup
- customThe title compound was prepared
- customPurification by flash chromatography (CHCl3/MeOH)
Sources & evidence
- ORD record
- ord-df38715c667c452c909d5a3bbaefaea1
- Source dataset
- uspto-grants-2011_08
- Patent number
- US08008302B2
Reaction notes
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