5-(2-amino-4-methoxy-phenylamino)-1H-[1,2,3]triazole-4-carboxylic acid amide

Base Information

Chemical Name:5-(2-amino-4-methoxy-phenylamino)-1H-[1,2,3]triazole-4-carboxylic acid amide
CAS No.:304874-16-6
Molecular Formula:C₁₀H₁₂N₆O₂
Molecular Weight:248.244
Hs Code.:

5-(2-amino-4-methoxy-phenylamino)-1<i>H</i>-[1,2,3]triazole-4-carboxylic acid amide

Synonyms:5-(2-amino-4-methoxy-phenylamino)-1H-[1,2,3]triazole-4-carboxylic acid amide

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Chemical Property of 5-(2-amino-4-methoxy-phenylamino)-1H-[1,2,3]triazole-4-carboxylic acid amide

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Technology Process of 5-(2-amino-4-methoxy-phenylamino)-1H-[1,2,3]triazole-4-carboxylic acid amide

There total 3 articles about 5-(2-amino-4-methoxy-phenylamino)-1H-[1,2,3]triazole-4-carboxylic acid amide 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: 86.0%

: 304874-10-0
4-carboxamido-5-(2-nitro-4-methoxy-anilino)-1,2,3-triazole

: 304874-16-6
5-(2-amino-4-methoxy-phenylamino)-1H-[1,2,3]triazole-4-carboxylic acid amide

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; at 20 ℃; under 760 Torr;
DOI:10.1016/S0223-5234(00)00180-X

Reference yield:

: 10336-13-7
1-azido-4-methoxy-2-nitrobenzene

: 304874-16-6
5-(2-amino-4-methoxy-phenylamino)-1H-[1,2,3]triazole-4-carboxylic acid amide

Guidance literature:: Multi-step reaction with 3 steps

1.1: NaOEt / ethanol

1.2: ethanol / -10 - 20 °C

2.1: aq. NaOH / Heating

3.1: 86 percent / H₂ / 10 percent Pd/C / methanol / 20 °C / 760 Torr

With sodium hydroxide; hydrogen; sodium ethanolate; palladium on activated charcoal; In methanol; ethanol; 1.1: Addition / 1.2: Cycloaddition / 2.1: Dimroth rearrangement / 3.1: Catalytic hydrogenation;
DOI:10.1016/S0223-5234(00)00180-X

Reference yield:

: 521959-53-5
1-(2-nitro-4-methoxy-phenyl)-4-carboxamido-5-amino-1H-1,2,3-triazole

: 304874-16-6
5-(2-amino-4-methoxy-phenylamino)-1H-[1,2,3]triazole-4-carboxylic acid amide

Guidance literature:: Multi-step reaction with 2 steps

1: aq. NaOH / Heating

2: 86 percent / H₂ / 10 percent Pd/C / methanol / 20 °C / 760 Torr

With sodium hydroxide; hydrogen; palladium on activated charcoal; In methanol; 1: Dimroth rearrangement / 2: Catalytic hydrogenation;
DOI:10.1016/S0223-5234(00)00180-X