4-(2-amino[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-fluoro-N-(4-fluorobenzyl)-benzamide

Base Information

Chemical Name:4-(2-amino[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-fluoro-N-(4-fluorobenzyl)-benzamide
CAS No.:1352620-84-8
Molecular Formula:C₂₀H₁₅F₂N₅O
Molecular Weight:379.369
Hs Code.:

Synonyms:4-(2-amino[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-fluoro-N-(4-fluorobenzyl)-benzamide

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Chemical Property of 4-(2-amino[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-fluoro-N-(4-fluorobenzyl)-benzamide

Chemical Property:

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Technology Process of 4-(2-amino[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-fluoro-N-(4-fluorobenzyl)-benzamide

There total 4 articles about 4-(2-amino[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-fluoro-N-(4-fluorobenzyl)-benzamide 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:

: 1309682-26-5
4-(2-amino[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-fluorobenzoic acid

: 140-75-0
para-fluorobenzylamine

: 1352620-84-8
4-(2-amino[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-fluoro-N-(4-fluorobenzyl)-benzamide

Guidance literature:: With potassium carbonate; HATU; In N,N-dimethyl-formamide; at 20 ℃; for 2h; Molecular sieve;

Reference yield:

: 1072-97-5
5-bromo-2-pyridylamine

: 1352620-84-8
4-(2-amino[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-fluoro-N-(4-fluorobenzyl)-benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: 1,4-dioxane / 2 h / 20 °C

2: hydroxylamine hydrochloride; N-ethyl-N,N-diisopropylamine / methanol / 2 h / 60 °C

3: potassium carbonate / triphenylphosphine; bis-triphenylphosphine-palladium(II) chloride / propan-1-ol / 2 h / Reflux

4: potassium carbonate; HATU / N,N-dimethyl-formamide / 2 h / 20 °C / Molecular sieve

With hydroxylamine hydrochloride; potassium carbonate; N-ethyl-N,N-diisopropylamine; HATU; bis-triphenylphosphine-palladium(II) chloride; triphenylphosphine; In 1,4-dioxane; methanol; propan-1-ol; N,N-dimethyl-formamide;

Reference yield:

: 947248-68-2
6-bromo-[1,2,4]triazolo[1,5-a]pyridin-2-amine

: 1352620-84-8
4-(2-amino[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-fluoro-N-(4-fluorobenzyl)-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / triphenylphosphine; bis-triphenylphosphine-palladium(II) chloride / propan-1-ol / 2 h / Reflux

2: potassium carbonate; HATU / N,N-dimethyl-formamide / 2 h / 20 °C / Molecular sieve

With potassium carbonate; HATU; bis-triphenylphosphine-palladium(II) chloride; triphenylphosphine; In propan-1-ol; N,N-dimethyl-formamide;