Benzo(B)Thiophene-2-Boronic Acid → HCID 57936186, compound
Reaction equation
Cl[C:2]1[N:7]=[C:6](Cl)[CH:5]=[CH:4][N:3]=1.[S:9]1[C:13](B(O)O)=[CH:12][C:11]2[CH:17]=[CH:18][CH:19]=[CH:20][C:10]1=2.[NH2:21][CH:22]1[CH2:27][C:26]([CH3:29])([CH3:28])[N:25]([OH:30])[C:24]([CH3:32])([CH3:31])[CH2:23]1>>[S:9]1[C:13]([C:6]2[CH:5]=[CH:4][N:3]=[C:2]([NH:21][CH:22]3[CH2:27][C:26]([CH3:28])([CH3:29])[N:25]([OH:30])[C:24]([CH3:32])([CH3:31])[CH2:23]3)[N:7]=2)=[CH:12][C:11]2[CH:17]=[CH:18][CH:19]=[CH:20][C:10]1=2Participants
4
Procedure
The title compound was prepared analogous to Method A, starting from 2,4-dichloro-pyrimidine, benzo[b]thiophen-2-boronic acid and 4-amino-2,2,6,6-tetramethylpiperidine-1-ol.
Sources & evidence
- ORD record
- ord-1652da7225f1439a8f1e2c9e2ce8d64e
- Source dataset
- uspto-grants-2009_11
- Patent number
- US07615562B2
Reaction notes
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