4-Chlorophenylboronic acid → 3-(4-Chlorophenyl)azetidine--hydrogen chloride (1/1)
Reaction equation
[ClH:1].[NH:2]1[CH2:5][CH:4]([C:6]2[CH:13]=[CH:12][C:9](C#N)=[CH:8][CH:7]=2)[CH2:3]1.[Cl:14]C1C=CC(B(O)O)=CC=1>>[ClH:14].[Cl:1][C:9]1[CH:12]=[CH:13][C:6]([CH:4]2[CH2:5][NH:2][CH2:3]2)=[CH:7][CH:8]=1Participants
3
Procedure
The title compound was prepared using standard chemical manipulations and procedures similar to those used for the preparation of compound 5.2, except (4-chlorophenyl)boronic acid was used in place of (4-cyanophenyl)boronic acid. The title compound was obtained in 20% yield over two steps.
Workup
- customThe title compound was prepared
Sources & evidence
- ORD record
- ord-2dbe2b6d1fe94abbbd11cae061fd2f6f
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09428502B2
Reaction notes
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