N-(3-chloro-4-fluorophenyl)-5-methyl-6-(3-(4-nitrophenyl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-yl)selenopheno[2,3-d]pyrimidin-4-amine

Base Information

Chemical Name:N-(3-chloro-4-fluorophenyl)-5-methyl-6-(3-(4-nitrophenyl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-yl)selenopheno[2,3-d]pyrimidin-4-amine
CAS No.:1578155-51-7
Molecular Formula:C₂₂H₁₂ClFN₈O₂SSe
Molecular Weight:585.867
Hs Code.:

Synonyms:N-(3-chloro-4-fluorophenyl)-5-methyl-6-(3-(4-nitrophenyl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-yl)selenopheno[2,3-d]pyrimidin-4-amine

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Chemical Property of N-(3-chloro-4-fluorophenyl)-5-methyl-6-(3-(4-nitrophenyl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-yl)selenopheno[2,3-d]pyrimidin-4-amine

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Technology Process of N-(3-chloro-4-fluorophenyl)-5-methyl-6-(3-(4-nitrophenyl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-yl)selenopheno[2,3-d]pyrimidin-4-amine

There total 8 articles about N-(3-chloro-4-fluorophenyl)-5-methyl-6-(3-(4-nitrophenyl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-yl)selenopheno[2,3-d]pyrimidin-4-amine 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: 61.0%

: 1380808-79-6
4-(3-chloro-4-fluorophenylamino)-5-methylselenopheno[2,3-d]pyrimidine-6-carboxylic acid

: 36209-50-4
4-amino-5-(4-nitrophenyl)-1,2,4-triazole-3-thiol

: 1578155-51-7
N-(3-chloro-4-fluorophenyl)-5-methyl-6-(3-(4-nitrophenyl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-yl)selenopheno[2,3-d]pyrimidin-4-amine

Guidance literature:: 4-(3-chloro-4-fluorophenylamino)-5-methylselenopheno[2,3-d]pyrimidine-6-carboxylic acid; 4-amino-5-(4-nitrophenyl)-1,2,4-triazole-3-thiol; With trichlorophosphate; Reflux;

With sodium hydroxide; at 20 ℃; for 2.15h; Cooling with ice;
DOI:10.1016/j.ejmech.2014.01.006

Reference yield:

: 1380809-71-1
ethyl 5-amino-4-cyano-3-methylselenophene-2-carboxylate

: 1578155-51-7
N-(3-chloro-4-fluorophenyl)-5-methyl-6-(3-(4-nitrophenyl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-yl)selenopheno[2,3-d]pyrimidin-4-amine

Guidance literature:: Multi-step reaction with 4 steps

1.1: 6 h / Reflux

2.1: acetic acid / 4 h / Reflux

3.1: sodium hydroxide / methanol; water / 16 h / 20 °C

3.2: 0.25 h

4.1: trichlorophosphate / Reflux

4.2: 2.15 h / 20 °C / Cooling with ice

With acetic acid; sodium hydroxide; trichlorophosphate; In methanol; water;
DOI:10.1016/j.ejmech.2014.01.006

Reference yield:

: 1482541-19-4
4-cyano-5-ethoxymethyleneimino-3-methylselenophene-2-carboxylic acid ethyl ester

: 1578155-51-7
N-(3-chloro-4-fluorophenyl)-5-methyl-6-(3-(4-nitrophenyl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-yl)selenopheno[2,3-d]pyrimidin-4-amine

Guidance literature:: Multi-step reaction with 3 steps

1.1: acetic acid / 4 h / Reflux

2.1: sodium hydroxide / methanol; water / 16 h / 20 °C

2.2: 0.25 h

3.1: trichlorophosphate / Reflux

3.2: 2.15 h / 20 °C / Cooling with ice

With acetic acid; sodium hydroxide; trichlorophosphate; In methanol; water;
DOI:10.1016/j.ejmech.2014.01.006