(1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)(pyridin-4-ylamino)gold

Base Information

Chemical Name:(1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)(pyridin-4-ylamino)gold
CAS No.:1522372-26-4
Molecular Formula:C₃₂H₄₁AuN₄
Molecular Weight:678.671
Hs Code.:

Synonyms:(1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)(pyridin-4-ylamino)gold

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Chemical Property of (1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)(pyridin-4-ylamino)gold

Chemical Property:

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Technology Process of (1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)(pyridin-4-ylamino)gold

There total 3 articles about (1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)(pyridin-4-ylamino)gold which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 88.0%

: 504-24-5
4-aminopyridine

: AuOH(1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)

: 1522372-26-4
(1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)(pyridin-4-ylamino)gold

Guidance literature:: In tetrahydrofuran; at 20 ℃; for 20h;
DOI:10.3762/bjoc.9.260

Reference yield:

: 250285-32-6
1,3-bis[2,6-diisopropylphenyl]imidazolium chloride

: 1522372-26-4
(1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)(pyridin-4-ylamino)gold

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate / acetone / 1 h / 60 °C

2: tetrahydrofuran / 20 h / 30 °C

3: tetrahydrofuran / 20 h / 20 °C

With potassium carbonate; In tetrahydrofuran; acetone;
DOI:10.3762/bjoc.9.260

Reference yield:

: chloro(1,3-bis(2,6-di-i-propylphenyl)imidazol-2-ylidene)gold(I)

: 1522372-26-4
(1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)(pyridin-4-ylamino)gold

Guidance literature:: Multi-step reaction with 2 steps

1: tetrahydrofuran / 20 h / 30 °C

2: tetrahydrofuran / 20 h / 20 °C

In tetrahydrofuran;
DOI:10.3762/bjoc.9.260