4-(4-(2-chlorophenyl)-5-((E)-2-(5-(2-methoxypyridin-4-yl)-1,3,4-oxadiazol-2-yl)vinyl)-4H-1,2,4-triazol-3-yl)pyridine

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Chemical Name:4-(4-(2-chlorophenyl)-5-((E)-2-(5-(2-methoxypyridin-4-yl)-1,3,4-oxadiazol-2-yl)vinyl)-4H-1,2,4-triazol-3-yl)pyridine
CAS No.:1380672-01-4
Molecular Formula:C₂₃H₁₆ClN₇O₂
Molecular Weight:457.879
Hs Code.:

Synonyms:4-(4-(2-chlorophenyl)-5-((E)-2-(5-(2-methoxypyridin-4-yl)-1,3,4-oxadiazol-2-yl)vinyl)-4H-1,2,4-triazol-3-yl)pyridine

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Chemical Property of 4-(4-(2-chlorophenyl)-5-((E)-2-(5-(2-methoxypyridin-4-yl)-1,3,4-oxadiazol-2-yl)vinyl)-4H-1,2,4-triazol-3-yl)pyridine

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Technology Process of 4-(4-(2-chlorophenyl)-5-((E)-2-(5-(2-methoxypyridin-4-yl)-1,3,4-oxadiazol-2-yl)vinyl)-4H-1,2,4-triazol-3-yl)pyridine

There total 2 articles about 4-(4-(2-chlorophenyl)-5-((E)-2-(5-(2-methoxypyridin-4-yl)-1,3,4-oxadiazol-2-yl)vinyl)-4H-1,2,4-triazol-3-yl)pyridine 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: 28.0%

: N-amino-N'-(2-chlorophenyl)pyridine-4-carboxamidine

: 1380672-63-8
(Z)-4-(2-methoxypyridine-4-carboamido)-4-oxobut-2-enoic acid

: 1380672-01-4
4-(4-(2-chlorophenyl)-5-((E)-2-(5-(2-methoxypyridin-4-yl)-1,3,4-oxadiazol-2-yl)vinyl)-4H-1,2,4-triazol-3-yl)pyridine

Guidance literature:: (Z)-4-(2-methoxypyridine-4-carboamido)-4-oxobut-2-enoic acid; With trichlorophosphate; In acetonitrile; at 20 ℃; for 16h; Reflux;

N-amino-N'-(2-chlorophenyl)pyridine-4-carboxamidine; With potassium carbonate; In acetonitrile; at 20 ℃; for 3h; Reflux;

Reference yield:

: 105596-63-2
2-methoxy-isonicotinic acid

: 1380672-01-4
4-(4-(2-chlorophenyl)-5-((E)-2-(5-(2-methoxypyridin-4-yl)-1,3,4-oxadiazol-2-yl)vinyl)-4H-1,2,4-triazol-3-yl)pyridine

Guidance literature:: Multi-step reaction with 3 steps

1.1: thionyl chloride / methanol / 2 h / 20 °C / Reflux

1.2: 0.5 h / Reflux

2.1: tetrahydrofuran / 16 h / 20 °C

3.1: trichlorophosphate / acetonitrile / 16 h / 20 °C / Reflux

3.2: 3 h / 20 °C / Reflux

With thionyl chloride; trichlorophosphate; In tetrahydrofuran; methanol; acetonitrile;