2-(4-fluorophenyl)-N-[4-(2-{[4-(morpholin-4-ylcarbonyl)-2-(2,2,2-trifluoro-ethoxy)phenyl]amino}[1,2,4]triazolo[1,5-a]pyridin-6-yl)phenyl]acetamide

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Chemical Name:2-(4-fluorophenyl)-N-[4-(2-{[4-(morpholin-4-ylcarbonyl)-2-(2,2,2-trifluoro-ethoxy)phenyl]amino}[1,2,4]triazolo[1,5-a]pyridin-6-yl)phenyl]acetamide
CAS No.:1352619-71-6
Molecular Formula:C₃₃H₂₈F₄N₆O₄
Molecular Weight:648.617
Hs Code.:

Synonyms:2-(4-fluorophenyl)-N-[4-(2-{[4-(morpholin-4-ylcarbonyl)-2-(2,2,2-trifluoro-ethoxy)phenyl]amino}[1,2,4]triazolo[1,5-a]pyridin-6-yl)phenyl]acetamide

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Chemical Property of 2-(4-fluorophenyl)-N-[4-(2-{[4-(morpholin-4-ylcarbonyl)-2-(2,2,2-trifluoro-ethoxy)phenyl]amino}[1,2,4]triazolo[1,5-a]pyridin-6-yl)phenyl]acetamide

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Technology Process of 2-(4-fluorophenyl)-N-[4-(2-{[4-(morpholin-4-ylcarbonyl)-2-(2,2,2-trifluoro-ethoxy)phenyl]amino}[1,2,4]triazolo[1,5-a]pyridin-6-yl)phenyl]acetamide

There total 3 articles about 2-(4-fluorophenyl)-N-[4-(2-{[4-(morpholin-4-ylcarbonyl)-2-(2,2,2-trifluoro-ethoxy)phenyl]amino}[1,2,4]triazolo[1,5-a]pyridin-6-yl)phenyl]acetamide 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%

: 1352621-13-6
[4-iodo-3-(2,2,2-trifluoroethoxy)phenyl](morpholin-4-yl)methanone

: 1352620-72-4
N-[4-(2-amino[1,2,4]triazolo[1,5-a]pyridin-6-yl)phenyl]-2-(4-fluorophenyl)-acetamide

: 1352619-71-6
2-(4-fluorophenyl)-N-[4-(2-{[4-(morpholin-4-ylcarbonyl)-2-(2,2,2-trifluoro-ethoxy)phenyl]amino}[1,2,4]triazolo[1,5-a]pyridin-6-yl)phenyl]acetamide

Guidance literature:: With sodium t-butanolate; chloro(2-dicyclohexylphosphino-2',4',6'-tri-i-propyl-1,1'-biphenyl)[2-(2-aminoethyl)phenyl]palladium(ll)methyl-t-butylether adduct; XPhos; In toluene; at 130 ℃; for 6h;

Reference yield:

: 58123-77-6
3-hydroxy-4-iodobenzoic acid

: 1352619-71-6
2-(4-fluorophenyl)-N-[4-(2-{[4-(morpholin-4-ylcarbonyl)-2-(2,2,2-trifluoro-ethoxy)phenyl]amino}[1,2,4]triazolo[1,5-a]pyridin-6-yl)phenyl]acetamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 0.17 h / 0 °C

1.2: 0 - 20 °C

2.1: potassium carbonate / N,N-dimethyl-formamide; acetonitrile / 0.5 h / 150 °C / Microwave irradiation

3.1: sodium t-butanolate / XPhos; chloro(2-dicyclohexylphosphino-2',4',6'-tri-i-propyl-1,1'-biphenyl)[2-(2-aminoethyl)phenyl]palladium(ll)methyl-t-butylether adduct / toluene / 6 h / 130 °C

With oxalyl dichloride; potassium carbonate; sodium t-butanolate; chloro(2-dicyclohexylphosphino-2',4',6'-tri-i-propyl-1,1'-biphenyl)[2-(2-aminoethyl)phenyl]palladium(ll)methyl-t-butylether adduct; N,N-dimethyl-formamide; XPhos; In dichloromethane; N,N-dimethyl-formamide; toluene; acetonitrile;

Reference yield:

: 1352621-12-5
(3-hydroxy-4-iodophenyl)(morpholin-4-yl)methanone

: 1352619-71-6
2-(4-fluorophenyl)-N-[4-(2-{[4-(morpholin-4-ylcarbonyl)-2-(2,2,2-trifluoro-ethoxy)phenyl]amino}[1,2,4]triazolo[1,5-a]pyridin-6-yl)phenyl]acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / N,N-dimethyl-formamide; acetonitrile / 0.5 h / 150 °C / Microwave irradiation

2: sodium t-butanolate / XPhos; chloro(2-dicyclohexylphosphino-2',4',6'-tri-i-propyl-1,1'-biphenyl)[2-(2-aminoethyl)phenyl]palladium(ll)methyl-t-butylether adduct / toluene / 6 h / 130 °C

With potassium carbonate; sodium t-butanolate; chloro(2-dicyclohexylphosphino-2',4',6'-tri-i-propyl-1,1'-biphenyl)[2-(2-aminoethyl)phenyl]palladium(ll)methyl-t-butylether adduct; XPhos; In N,N-dimethyl-formamide; toluene; acetonitrile;