N-{1-[3-(2-Ethoxyphenyl)-5-oxo-4,5-dihydro-[1,2,4]triazin-6-yl]ethyl}oxalamic acid ethyl ester

Base Information

Chemical Name:N-{1-[3-(2-Ethoxyphenyl)-5-oxo-4,5-dihydro-[1,2,4]triazin-6-yl]ethyl}oxalamic acid ethyl ester
CAS No.:1417529-65-7
Molecular Formula:C₁₇H₂₀N₄O₅
Molecular Weight:360.37
Hs Code.:

Synonyms:N-{1-[3-(2-Ethoxyphenyl)-5-oxo-4,5-dihydro-[1,2,4]triazin-6-yl]ethyl}oxalamic acid ethyl ester

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Chemical Property of N-{1-[3-(2-Ethoxyphenyl)-5-oxo-4,5-dihydro-[1,2,4]triazin-6-yl]ethyl}oxalamic acid ethyl ester

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Technology Process of N-{1-[3-(2-Ethoxyphenyl)-5-oxo-4,5-dihydro-[1,2,4]triazin-6-yl]ethyl}oxalamic acid ethyl ester

There total 3 articles about N-{1-[3-(2-Ethoxyphenyl)-5-oxo-4,5-dihydro-[1,2,4]triazin-6-yl]ethyl}oxalamic acid ethyl ester 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:

: 93-89-0,99341-95-4
benzoic acid ethyl ester

: 1417529-56-6
C₁₃H₁₆N₄O₂

: 1417529-65-7
N-{1-[3-(2-Ethoxyphenyl)-5-oxo-4,5-dihydro-[1,2,4]triazin-6-yl]ethyl}oxalamic acid ethyl ester

Guidance literature:: C₁₃H₁₆N₄O₂; With tertiary amine; In dichloromethane; for 0.0833333h; Cooling;

benzoic acid ethyl ester; In dichloromethane; at 0 - 20 ℃; for 1.16667h;
DOI:10.1016/j.tet.2012.11.037

Reference yield:

: 1417529-52-2
3-(2-ethoxyphenyl)-6-ethyl-4H-[1,2,4]triazin-5-one

: 1417529-65-7
N-{1-[3-(2-Ethoxyphenyl)-5-oxo-4,5-dihydro-[1,2,4]triazin-6-yl]ethyl}oxalamic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 14 h / Reflux; Inert atmosphere

2.1: ammonia / tetrahydrofuran / 20 °C

3.1: tertiary amine / dichloromethane / 0.08 h / Cooling

3.2: 1.17 h / 0 - 20 °C

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); ammonia; In tetrahydrofuran; tetrachloromethane; dichloromethane;
DOI:10.1016/j.tet.2012.11.037

Reference yield:

: 1417529-54-4
6-(1-bromoethyl)-3-(2-ethoxyphenyl)-4H-[1,2,4]triazin-5-one

: 1417529-65-7
N-{1-[3-(2-Ethoxyphenyl)-5-oxo-4,5-dihydro-[1,2,4]triazin-6-yl]ethyl}oxalamic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: ammonia / tetrahydrofuran / 20 °C

2.1: tertiary amine / dichloromethane / 0.08 h / Cooling

2.2: 1.17 h / 0 - 20 °C

With ammonia; In tetrahydrofuran; dichloromethane;
DOI:10.1016/j.tet.2012.11.037