2-(4,4-dimethylpiperidin-1-yl)-4-((5-methyl-3-(5-phenyl-1,3,4-oxadiazol-2-yl)-1H-1,2,4-triazol-1-yl)methyl)pyridin-1-ium trifluoroacetate

Base Information

Chemical Name:2-(4,4-dimethylpiperidin-1-yl)-4-((5-methyl-3-(5-phenyl-1,3,4-oxadiazol-2-yl)-1H-1,2,4-triazol-1-yl)methyl)pyridin-1-ium trifluoroacetate
CAS No.:1570493-97-8
Molecular Formula:C₂HF₃O₂*C₂₄H₂₇N₇O
Molecular Weight:543.549
Hs Code.:

Synonyms:2-(4,4-dimethylpiperidin-1-yl)-4-((5-methyl-3-(5-phenyl-1,3,4-oxadiazol-2-yl)-1H-1,2,4-triazol-1-yl)methyl)pyridin-1-ium trifluoroacetate

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Chemical Property of 2-(4,4-dimethylpiperidin-1-yl)-4-((5-methyl-3-(5-phenyl-1,3,4-oxadiazol-2-yl)-1H-1,2,4-triazol-1-yl)methyl)pyridin-1-ium trifluoroacetate

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Technology Process of 2-(4,4-dimethylpiperidin-1-yl)-4-((5-methyl-3-(5-phenyl-1,3,4-oxadiazol-2-yl)-1H-1,2,4-triazol-1-yl)methyl)pyridin-1-ium trifluoroacetate

There total 3 articles about 2-(4,4-dimethylpiperidin-1-yl)-4-((5-methyl-3-(5-phenyl-1,3,4-oxadiazol-2-yl)-1H-1,2,4-triazol-1-yl)methyl)pyridin-1-ium trifluoroacetate 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: 27.0%

: 1570494-02-8
2-(1-((2-chloropyridin-4-yl)methyl)-5-methyl-1H-1,2,4-triazol-3-yl)-5-phenyl-1,3,4-oxadiazole

: 38646-68-3
4,4-dimethylpiperidine hydrochloric acid salt

: 76-05-1
trifluoroacetic acid

: 1570493-97-8
2-(4,4-dimethylpiperidin-1-yl)-4-((5-methyl-3-(5-phenyl-1,3,4-oxadiazol-2-yl)-1H-1,2,4-triazol-1-yl)methyl)pyridin-1-ium trifluoroacetate

Guidance literature:: 2-(1-((2-chloropyridin-4-yl)methyl)-5-methyl-1H-1,2,4-triazol-3-yl)-5-phenyl-1,3,4-oxadiazole; 4,4-dimethylpiperidine hydrochloric acid salt; With N-ethyl-N,N-diisopropylamine; In dimethyl sulfoxide; at 120 ℃;

trifluoroacetic acid; In water; acetonitrile;

Reference yield:

: 99367-59-6
5-phenyl-1,3,4-oxadiazole-2-carbohydrazide

: 1570493-97-8
2-(4,4-dimethylpiperidin-1-yl)-4-((5-methyl-3-(5-phenyl-1,3,4-oxadiazol-2-yl)-1H-1,2,4-triazol-1-yl)methyl)pyridin-1-ium trifluoroacetate

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydroxide / 5,5-dimethyl-1,3-cyclohexadiene / 36 h / 170 °C

2.1: caesium carbonate; sodium iodide / N,N-dimethyl-formamide / 20 °C

3.1: N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 120 °C

3.2: Waters C₁₈

With caesium carbonate; N-ethyl-N,N-diisopropylamine; sodium iodide; sodium hydroxide; In 5,5-dimethyl-1,3-cyclohexadiene; dimethyl sulfoxide; N,N-dimethyl-formamide;

Reference yield:

: 1570493-99-0
2-(5-methyl-1H-1,2,4-triazol-3-yl)-5-phenyl-1,3,4-oxadiazole

: 1570493-97-8
2-(4,4-dimethylpiperidin-1-yl)-4-((5-methyl-3-(5-phenyl-1,3,4-oxadiazol-2-yl)-1H-1,2,4-triazol-1-yl)methyl)pyridin-1-ium trifluoroacetate

Guidance literature:: Multi-step reaction with 2 steps

1.1: caesium carbonate; sodium iodide / N,N-dimethyl-formamide / 20 °C

2.1: N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 120 °C

2.2: Waters C₁₈

With caesium carbonate; N-ethyl-N,N-diisopropylamine; sodium iodide; In dimethyl sulfoxide; N,N-dimethyl-formamide;