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Merck
CN

902039

Sigma-Aldrich

4-Methoxypicolinimidamide hydrochloride

≥95%

别名:

Weix 2-pyridylcarboxamidine ligand for nickel catalysis

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About This Item

经验公式(希尔记法):
C7H10ClN3O
分子量:
187.63
MDL编号:
UNSPSC代码:
12352101
NACRES:
NA.22

检测方案

≥95%

形式

powder or solid

反应适用性

core: nickel
reaction type: Cross Couplings
reagent type: catalyst

mp

174-176 °C

InChI

1S/C7H9N3O.ClH/c1-11-5-2-3-10-6(4-5)7(8)9;/h2-4H,1H3,(H3,8,9);1H

InChI key

JOUDWIBACXLPIO-UHFFFAOYSA-N

应用

This pyridyl carboxamidine ligand has been demonstrated by Daniel Weix′s lab to enable nickel-catalyzed cross-coupling of diverse basic nitrogen heterocycles with primary and secondary alkyl halides.

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Eric C Hansen et al.
Nature chemistry, 8(12), 1126-1130 (2016-11-23)
Ligands are essential for controlling the reactivity and selectivity of reactions catalysed by transition metals. Access to large phosphine ligand libraries has become an essential tool for the application of metal-catalysed reactions industrially, but these existing libraries are not well
Eric C Hansen et al.
The Journal of organic chemistry, 82(14), 7085-7092 (2017-07-07)
Despite their importance, the synthesis of alkylated heterocycles from the cross-coupling of Lewis basic nitrogen heteroaryl halides with alkyl halides remains a challenge. We report here a general solution to this challenge enabled by a new collection of ligands based
Robert J Perkins et al.
Organic letters, 19(14), 3755-3758 (2017-07-14)
A constant-current electrochemical method for reducing catalytic nickel complexes in sp2-sp3 cross-electrophile coupling reactions has been developed. The electrochemical reduction provides reliable nickel catalyst activation and turnover and offers a tunable parameter for reaction optimization, in contrast to more standard

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