N'-acetoxy-2-[4-(4-tert-butylphenyl)-2-oxopyridin-1(2H)-yl]ethanimidamide

Base Information

Chemical Name:N'-acetoxy-2-[4-(4-tert-butylphenyl)-2-oxopyridin-1(2H)-yl]ethanimidamide
CAS No.:1192165-07-3
Molecular Formula:C₁₉H₂₃N₃O₃
Molecular Weight:341.41
Hs Code.:

Synonyms:N'-acetoxy-2-[4-(4-tert-butylphenyl)-2-oxopyridin-1(2H)-yl]ethanimidamide

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Chemical Property of N'-acetoxy-2-[4-(4-tert-butylphenyl)-2-oxopyridin-1(2H)-yl]ethanimidamide

Chemical Property:

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Technology Process of N'-acetoxy-2-[4-(4-tert-butylphenyl)-2-oxopyridin-1(2H)-yl]ethanimidamide

There total 3 articles about N'-acetoxy-2-[4-(4-tert-butylphenyl)-2-oxopyridin-1(2H)-yl]ethanimidamide 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:

: 1192165-08-4
2-[4-(4-tert-butylphenyl)-2-oxopyridin-1(2H)-yl]-N'-(hydroxy)ethanimidamide

: 108-24-7
acetic anhydride

: 1192165-07-3
N'-acetoxy-2-[4-(4-tert-butylphenyl)-2-oxopyridin-1(2H)-yl]ethanimidamide

Guidance literature:: With triethylamine; In 1,4-dioxane; at 20 ℃; for 3h;

Reference yield:

: 1192165-05-1
[4-(4-tert-Butylphenyl)-2-oxopyridin-1(2H)-yl]acetonitrile

: 1192165-07-3
N'-acetoxy-2-[4-(4-tert-butylphenyl)-2-oxopyridin-1(2H)-yl]ethanimidamide

Guidance literature:: Multi-step reaction with 2 steps

1: hydroxylamine / ethanol; water / 1 h / Reflux

2: triethylamine / 1,4-dioxane / 3 h / 20 °C

With hydroxylamine; triethylamine; In 1,4-dioxane; ethanol; water;

Reference yield:

: 942947-02-6
2-(benzyloxy)-4-(4-tert-butylphenyl)pyridine

: 1192165-07-3
N'-acetoxy-2-[4-(4-tert-butylphenyl)-2-oxopyridin-1(2H)-yl]ethanimidamide

Guidance literature:: Multi-step reaction with 3 steps

1: acetonitrile / 13 h / Reflux; Inert atmosphere

2: hydroxylamine / ethanol; water / 1 h / Reflux

3: triethylamine / 1,4-dioxane / 3 h / 20 °C

With hydroxylamine; triethylamine; In 1,4-dioxane; ethanol; water; acetonitrile;