trans-4-(2-amino-5-bromo-4-oxo-3,4-dihydroimidazo[5,1-f][1,2,4]triazin-7-yl)cyclohexanecarboxylic acid methyl ester

Base Information

Chemical Name:trans-4-(2-amino-5-bromo-4-oxo-3,4-dihydroimidazo[5,1-f][1,2,4]triazin-7-yl)cyclohexanecarboxylic acid methyl ester
CAS No.:1260585-94-1
Molecular Formula:C₁₃H₁₆BrN₅O₃
Molecular Weight:370.206
Hs Code.:

Synonyms:trans-4-(2-amino-5-bromo-4-oxo-3,4-dihydroimidazo[5,1-f][1,2,4]triazin-7-yl)cyclohexanecarboxylic acid methyl ester

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Chemical Property of trans-4-(2-amino-5-bromo-4-oxo-3,4-dihydroimidazo[5,1-f][1,2,4]triazin-7-yl)cyclohexanecarboxylic acid methyl ester

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Technology Process of trans-4-(2-amino-5-bromo-4-oxo-3,4-dihydroimidazo[5,1-f][1,2,4]triazin-7-yl)cyclohexanecarboxylic acid methyl ester

There total 4 articles about trans-4-(2-amino-5-bromo-4-oxo-3,4-dihydroimidazo[5,1-f][1,2,4]triazin-7-yl)cyclohexanecarboxylic acid methyl 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: 79.0%

: 936902-01-1
trans-4-(2-amino-4-oxo-3,4-dihydroimidazo[5,1-f][1,2,4]triazin-7-yl)cyclohexanecarboxylic acid methyl ester

: 1260585-94-1
trans-4-(2-amino-5-bromo-4-oxo-3,4-dihydroimidazo[5,1-f][1,2,4]triazin-7-yl)cyclohexanecarboxylic acid methyl ester

Guidance literature:: With N-Bromosuccinimide; In N,N-dimethyl-formamide; at 20 - 37 ℃; Industry scale;

Reference yield:

: 93206-03-2
3-amino-6-((dibenzylamino)methyl)-1,2,4-triazine-5-(4H)-one

: 1260585-94-1
trans-4-(2-amino-5-bromo-4-oxo-3,4-dihydroimidazo[5,1-f][1,2,4]triazin-7-yl)cyclohexanecarboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: hydrogen; acetic acid / palladium 10% on activated carbon / water / 55 °C / Industry scale; Inert atmosphere

1.2: Industry scale

1.3: 50 °C / Industry scale

2.1: trichlorophosphate / acetonitrile / Reflux; Industry scale

2.2: 1 h / 0 - 30 °C / pH 8 / Industry scale

3.1: N-Bromosuccinimide / N,N-dimethyl-formamide / 20 - 37 °C / Industry scale

With N-Bromosuccinimide; hydrogen; acetic acid; trichlorophosphate; palladium 10% on activated carbon; In water; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 103-49-1
dibenzylamine

: 1260585-94-1
trans-4-(2-amino-5-bromo-4-oxo-3,4-dihydroimidazo[5,1-f][1,2,4]triazin-7-yl)cyclohexanecarboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: ethyl acetate / 60 - 80 °C / Industry scale

1.2: 24 h / Reflux; Industry scale

2.1: hydrogen; acetic acid / palladium 10% on activated carbon / water / 55 °C / Industry scale; Inert atmosphere

2.2: Industry scale

2.3: 50 °C / Industry scale

3.1: trichlorophosphate / acetonitrile / Reflux; Industry scale

3.2: 1 h / 0 - 30 °C / pH 8 / Industry scale

4.1: N-Bromosuccinimide / N,N-dimethyl-formamide / 20 - 37 °C / Industry scale

With N-Bromosuccinimide; hydrogen; acetic acid; trichlorophosphate; palladium 10% on activated carbon; In water; ethyl acetate; N,N-dimethyl-formamide; acetonitrile;