5-Benzyl-8-oxo-3-pyrrolidin-1-yl-5,8-dihydro-pyrido[2,3-e][1,2,4]triazine-7-carboxylic acid ethyl ester

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Chemical Name:5-Benzyl-8-oxo-3-pyrrolidin-1-yl-5,8-dihydro-pyrido[2,3-e][1,2,4]triazine-7-carboxylic acid ethyl ester
CAS No.:75824-45-2
Molecular Formula:C₂₀H₂₁N₅O₃
Molecular Weight:379.418
Hs Code.:
Mol file:75824-45-2.mol

Synonyms:5-Benzyl-8-oxo-3-pyrrolidin-1-yl-5,8-dihydro-pyrido[2,3-e][1,2,4]triazine-7-carboxylic acid ethyl ester

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Chemical Property of 5-Benzyl-8-oxo-3-pyrrolidin-1-yl-5,8-dihydro-pyrido[2,3-e][1,2,4]triazine-7-carboxylic acid ethyl ester Edit

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Technology Process of 5-Benzyl-8-oxo-3-pyrrolidin-1-yl-5,8-dihydro-pyrido[2,3-e][1,2,4]triazine-7-carboxylic acid ethyl ester

There total 3 articles about 5-Benzyl-8-oxo-3-pyrrolidin-1-yl-5,8-dihydro-pyrido[2,3-e][1,2,4]triazine-7-carboxylic 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:

: 75824-13-4
5-Benzyl-8-hydroxy-3-methylsulfanyl-5,6-dihydro-pyrido[2,3-e][1,2,4]triazine-7-carboxylic acid ethyl ester

: 75824-45-2
5-Benzyl-8-oxo-3-pyrrolidin-1-yl-5,8-dihydro-pyrido[2,3-e][1,2,4]triazine-7-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 58 percent / triiethylamine, brome / CHCl₃ / 3 h / Ambient temperature

2: ethanol / 1 h / Heating

With bromine; triethylamine; In ethanol; chloroform;

Reference yield:

: 75824-07-6
5-[Benzyl-(2-ethoxycarbonyl-ethyl)-amino]-3-methylsulfanyl-[1,2,4]triazine-6-carboxylic acid ethyl ester

: 75824-45-2
5-Benzyl-8-oxo-3-pyrrolidin-1-yl-5,8-dihydro-pyrido[2,3-e][1,2,4]triazine-7-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 71 percent / 1.) potassium, alcool butylique tertiaire, 2.) acide acetique / toluene / 3 h / Ambient temperature

2: 58 percent / triiethylamine, brome / CHCl₃ / 3 h / Ambient temperature

3: ethanol / 1 h / Heating

With alcool butylique tertiaire; bromine; potassium; acetic acid; triethylamine; In ethanol; chloroform; toluene;