(Pyridin-4-yl)boronic acid → 4-Pyridin-4-yl-1H-indole-2-carboxylic acid [1-(2-azepan-1-yl-ethyl)piperidin-4-yl]-amide

HRID 2267937Notes

Reaction equation

HRID 2267937 reaction equation
[N:1]1([CH2:8][CH2:9][N:10]2[CH2:15][CH2:14][CH:13]([NH:16][C:17]([C:19]3[NH:20][C:21]4[C:26]([CH:27]=3)=[C:25](Br)[CH:24]=[CH:23][CH:22]=4)=[O:18])[CH2:12][CH2:11]2)[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[N:29]1[CH:34]=[CH:33][C:32](B(O)O)=[CH:31][CH:30]=1>>[N:1]1([CH2:8][CH2:9][N:10]2[CH2:15][CH2:14][CH:13]([NH:16][C:17]([C:19]3[NH:20][C:21]4[C:26]([CH:27]=3)=[C:25]([C:32]3[CH:33]=[CH:34][N:29]=[CH:30][CH:31]=3)[CH:24]=[CH:23][CH:22]=4)=[O:18])[CH2:12][CH2:11]2)[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1

Participants

3

Reactant 2

HCID 2734379(Pyridin-4-yl)boronic acidHCID 596002484-Bromo-1H-indole-2-carboxylic acid [1-(2-azepan-1-yl-ethyl)-piperidin-4-yl]-amide

Product 1

HCID 596002054-Pyridin-4-yl-1H-indole-2-carboxylic acid [1-(2-azepan-1-yl-ethyl)piperidin-4-yl]-amide

Procedure

This compound is synthesized from compound 194 (see example 156) and pyridin-4-yl-boronic acid analogously to the method described in Example 156.

Sources & evidence

ORD record
ord-585d9e179f494649b584e4506bb71264
Source dataset
uspto-grants-2010_12
Patent number
US07858781B2

Reaction notes

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