5-Methoxypyridine-3-boronic Acid → HCID 89442563, compound

HRID 2283988Notes

Reaction equation

HRID 2283988 reaction equation
FC1C=CC([C:8]2[C:9]([NH2:37])=[N:10][CH:11]=[N:12][C:13]=2[N:14]2[CH2:19][CH2:18][CH:17]([C:20]3[N:21]([CH3:36])[CH:22]=[C:23]([C:25]4[CH:30]=[CH:29][C:28]([F:31])=[C:27]([C:32]([F:35])([F:34])[F:33])[CH:26]=4)[N:24]=3)[CH2:16][CH2:15]2)=CC=1.[CH3:38][O:39][C:40]1[CH:41]=[C:42](B(O)O)[CH:43]=[N:44][CH:45]=1>>[F:31][C:28]1[CH:29]=[CH:30][C:25]([C:23]2[N:24]=[C:20]([CH:17]3[CH2:16][CH2:15][N:14]([C:13]4[N:12]=[CH:11][N:10]=[C:9]([NH2:37])[C:8]=4[C:42]4[CH:43]=[N:44][CH:45]=[C:40]([O:39][CH3:38])[CH:41]=4)[CH2:19][CH2:18]3)[N:21]([CH3:36])[CH:22]=2)=[CH:26][C:27]=1[C:32]([F:34])([F:33])[F:35]

Participants

3

Procedure

The title compound was prepared in an analogous manner as 5-(4-Fluoro-phenyl)-6-{4-[4-(4-fluoro-3-trifluoromethyl-phenyl)-1-methyl-1H-imidazol-2-yl]-piperidin-1-yl}-pyrimidin-4-ylamine using (5-methoxypyridin-3-yl)boronic acid instead of 4-fluorophenylboronic acid. LC-MS: (M+1=528, obsd.=528).

Sources & evidence

ORD record
ord-0fa158d407b24d9eb64f4b868bbbb732
Source dataset
uspto-grants-2015_09
Patent number
US09145392B2

Reaction notes

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