4-Chlorophenylboronic acid → (S)-3-Amino-1-(4-chlorophenyl)azepan-2-one hydrochloride
Reaction equation
Cl.[NH2:2][C@H:3]1[CH2:9][CH2:8][CH2:7][CH2:6][N:5]([C:10]2[CH:15]=[CH:14][CH:13]=[C:12]([Cl:16])[CH:11]=2)[C:4]1=[O:17].[Cl:18]C1C=CC(B(O)O)=CC=1>>[ClH:16].[NH2:2][C@H:3]1[CH2:9][CH2:8][CH2:7][CH2:6][N:5]([C:10]2[CH:15]=[CH:14][C:13]([Cl:18])=[CH:12][CH:11]=2)[C:4]1=[O:17]Participants
3
Procedure
(S)-3-Amino-1-(4-chlorophenyl)azepan-2-one hydrochloride (35 mg, 0.127 mmol) was synthesized as described for the preparation of Intermediate 49 using 4-chlorophenylboronic acid in step A. Anal. Calcd. for C12H15ClN2O m/z 238.8. found: 239.2 (M+H)+.
Sources & evidence
- ORD record
- ord-edfda83a2ccd40babafe5ca6596d97b0
- Source dataset
- uspto-grants-2016_05
- Patent number
- US09346852B2
Reaction notes
Loading…