2-(Trifluoromethyl)pyridine-5-boronic Acid → HCID 76314705, compound

HRID 512858Notes

Reaction equation

HRID 512858 reaction equation
[F:1][C:2]([F:13])([F:12])[C:3]1[CH:8]=[CH:7][C:6](B(O)O)=[CH:5][N:4]=1.Cl[C:15]1[N:20]=[N:19][C:18]([N:21]2[CH2:26][CH2:25][CH:24]([N:27]3[C:35]4[C:30](=[CH:31][CH:32]=[C:33]([F:36])[CH:34]=4)[CH2:29][CH2:28]3)[CH2:23][CH2:22]2)=[CH:17][CH:16]=1>>[F:36][C:33]1[CH:34]=[C:35]2[C:30]([CH2:29][CH2:28][N:27]2[CH:24]2[CH2:25][CH2:26][N:21]([C:18]3[N:19]=[N:20][C:15]([C:6]4[CH:5]=[N:4][C:3]([C:2]([F:13])([F:12])[F:1])=[CH:8][CH:7]=4)=[CH:16][CH:17]=3)[CH2:22][CH2:23]2)=[CH:31][CH:32]=1

Participants

3

Reactant 2

HCID 251342782-(Trifluoromethyl)pyridine-5-boronic AcidHCID 896144661-(1-(6-Chloropyridazin-3-yl)piperidin-4-yl)-6-fluoroindoline

Product 1

HCID 76314705HCID 76314705, compound

Procedure

The title compound was prepared following the procedure as described in Example 1, Method A, STEP 4, reacting 2-trifluoromethylpyridine-5-boronic acid and 1-(1-(6-chloropyridazin-3-yl)piperidin-4-yl)-6-fluoroindoline.

Sources & evidence

ORD record
ord-fe9b8b03019a40aa9d2d414a5872fa4b
Source dataset
uspto-grants-2015_08
Patent number
US09102669B2

Reaction notes

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