3-Pyridinylboronic acid → HCID 178420774, compound

HRID 2100992Notes

Reaction equation

HRID 2100992 reaction equation
Cl[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[C:4]([NH:12][C:13]2[CH:17]=[CH:16][NH:15][N:14]=2)[N:3]=1.[N:18]1[CH:23]=[CH:22][CH:21]=[C:20](B(O)O)[CH:19]=1>>[NH:15]1[CH:16]=[CH:17][C:13]([NH:12][C:4]2[N:3]=[C:2]([C:20]3[CH:19]=[N:18][CH:23]=[CH:22][CH:21]=3)[C:11]3[C:6]([CH:5]=2)=[CH:7][CH:8]=[CH:9][CH:10]=3)=[N:14]1

Participants

3

Reactant 2

HCID 27343783-Pyridinylboronic acidHCID 178478391HCID 178478391, compound

Product 1

HCID 178420774HCID 178420774, compound

Procedure

Similar procedure as described in example 131 was used, starting from (1-chloro-isoquinolin-3-yl)-(1H-pyrazol-3-yl)-amine and 3-pyridinylboronic acid to give (1H-pyrazol-3-yl)-(1-pyridin-3-yl-isoquinolin-3-yl)-amine. LC-MS m/e 288(MH+).

Sources & evidence

ORD record
ord-393c6469a01744699f6439477f0e2d0f
Source dataset
uspto-grants-2009_08
Patent number
US07572809B2

Reaction notes

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