N-(4-(4-(5-methyl-1H-pyrazol-3-ylamino)-6-nitropyrrolo[2,1-f][1,2,4]triazin-2-ylthio)phenyl)cyclopropanecarboxamide

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Chemical Name:N-(4-(4-(5-methyl-1H-pyrazol-3-ylamino)-6-nitropyrrolo[2,1-f][1,2,4]triazin-2-ylthio)phenyl)cyclopropanecarboxamide
CAS No.:1315587-55-3
Molecular Formula:C₂₀H₁₈N₈O₃S
Molecular Weight:450.481
Hs Code.:

Synonyms:N-(4-(4-(5-methyl-1H-pyrazol-3-ylamino)-6-nitropyrrolo[2,1-f][1,2,4]triazin-2-ylthio)phenyl)cyclopropanecarboxamide

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Chemical Property of N-(4-(4-(5-methyl-1H-pyrazol-3-ylamino)-6-nitropyrrolo[2,1-f][1,2,4]triazin-2-ylthio)phenyl)cyclopropanecarboxamide

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Technology Process of N-(4-(4-(5-methyl-1H-pyrazol-3-ylamino)-6-nitropyrrolo[2,1-f][1,2,4]triazin-2-ylthio)phenyl)cyclopropanecarboxamide

There total 6 articles about N-(4-(4-(5-methyl-1H-pyrazol-3-ylamino)-6-nitropyrrolo[2,1-f][1,2,4]triazin-2-ylthio)phenyl)cyclopropanecarboxamide 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: 39.0%

: 639090-54-3
(N-(4-mercaptophenyl)cyclopropylcarboxamide)

: 1315587-54-2
2-chloro-N-(5-methyl-1H-pyrazol-3-yl)-6-nitropyrrolo[2,1-f][1,2,4]triazin-4-amine

: 1315587-55-3
N-(4-(4-(5-methyl-1H-pyrazol-3-ylamino)-6-nitropyrrolo[2,1-f][1,2,4]triazin-2-ylthio)phenyl)cyclopropanecarboxamide

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 60 ℃;

Reference yield:

: 1204245-52-2
1-amino-4-nitro-1H-pyrrole-2-carboxamide

: 1315587-55-3
N-(4-(4-(5-methyl-1H-pyrazol-3-ylamino)-6-nitropyrrolo[2,1-f][1,2,4]triazin-2-ylthio)phenyl)cyclopropanecarboxamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: pyridine / 1,4-dioxane / 1 h / Reflux

2.1: triethylamine; trichlorophosphate / Inert atmosphere; Reflux

3.1: potassium iodide / N,N-dimethyl-formamide / 0.08 h / 20 °C

3.2: 2 h / 20 °C

4.1: potassium carbonate / N,N-dimethyl-formamide / 60 °C

With pyridine; potassium carbonate; triethylamine; potassium iodide; trichlorophosphate; In 1,4-dioxane; N,N-dimethyl-formamide;

Reference yield:

: 1245644-73-8
6-nitropyrrolo[2,1-f][1,2,4]triazine-2,4(1H,3H)-dione

: 1315587-55-3
N-(4-(4-(5-methyl-1H-pyrazol-3-ylamino)-6-nitropyrrolo[2,1-f][1,2,4]triazin-2-ylthio)phenyl)cyclopropanecarboxamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine; trichlorophosphate / Inert atmosphere; Reflux

2.1: potassium iodide / N,N-dimethyl-formamide / 0.08 h / 20 °C

2.2: 2 h / 20 °C

3.1: potassium carbonate / N,N-dimethyl-formamide / 60 °C

With potassium carbonate; triethylamine; potassium iodide; trichlorophosphate; In N,N-dimethyl-formamide;