N,N-diethyl-4-{[6-(4-{[(4-fluorophenyl)acetyl]amino}phenyl)[1,2,4]triazolo[1,5-a]pyridin-2-yl]amino}-3-(2-methoxyethoxy)benzamide

Base Information

Chemical Name:N,N-diethyl-4-{[6-(4-{[(4-fluorophenyl)acetyl]amino}phenyl)[1,2,4]triazolo[1,5-a]pyridin-2-yl]amino}-3-(2-methoxyethoxy)benzamide
CAS No.:1403330-58-4
Molecular Formula:C₃₄H₃₅FN₆O₄
Molecular Weight:610.688
Hs Code.:

Synonyms:N,N-diethyl-4-{[6-(4-{[(4-fluorophenyl)acetyl]amino}phenyl)[1,2,4]triazolo[1,5-a]pyridin-2-yl]amino}-3-(2-methoxyethoxy)benzamide

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Chemical Property of N,N-diethyl-4-{[6-(4-{[(4-fluorophenyl)acetyl]amino}phenyl)[1,2,4]triazolo[1,5-a]pyridin-2-yl]amino}-3-(2-methoxyethoxy)benzamide

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Technology Process of N,N-diethyl-4-{[6-(4-{[(4-fluorophenyl)acetyl]amino}phenyl)[1,2,4]triazolo[1,5-a]pyridin-2-yl]amino}-3-(2-methoxyethoxy)benzamide

There total 3 articles about N,N-diethyl-4-{[6-(4-{[(4-fluorophenyl)acetyl]amino}phenyl)[1,2,4]triazolo[1,5-a]pyridin-2-yl]amino}-3-(2-methoxyethoxy)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: 12.0%

: 887412-13-7
N,N-diethyl-4-iodo-3-(2-methoxyethoxy)benzamide

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

: 1403330-58-4
N,N-diethyl-4-{[6-(4-{[(4-fluorophenyl)acetyl]amino}phenyl)[1,2,4]triazolo[1,5-a]pyridin-2-yl]amino}-3-(2-methoxyethoxy)benzamide

Guidance literature:: With sodium t-butanolate; chloro(2-dicyclohexylphosphino-2’,4’,6’-tri-i-propyl-1,1‘-biphenyl)[2-(2-aminoethyl)phenyl]palladium(II) methyl-t-butyl ether adduct; XPhos; In toluene; at 130 ℃; for 8h;

Reference yield:

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

: 1403330-58-4
N,N-diethyl-4-{[6-(4-{[(4-fluorophenyl)acetyl]amino}phenyl)[1,2,4]triazolo[1,5-a]pyridin-2-yl]amino}-3-(2-methoxyethoxy)benzamide

Guidance literature:: Multi-step reaction with 3 steps

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

1.2: 1.5 h / 20 °C

2.1: potassium carbonate / N,N-dimethyl-formamide; acetonitrile / 1 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(II) methyl-t-butyl ether adduct / toluene / 8 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(II) methyl-t-butyl ether adduct; N,N-dimethyl-formamide; XPhos; In dichloromethane; N,N-dimethyl-formamide; toluene; acetonitrile;

Reference yield:

: 911228-76-7
N,N-diethyl-3-hydroxy-4-iodobenzamide

: 1403330-58-4
N,N-diethyl-4-{[6-(4-{[(4-fluorophenyl)acetyl]amino}phenyl)[1,2,4]triazolo[1,5-a]pyridin-2-yl]amino}-3-(2-methoxyethoxy)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / N,N-dimethyl-formamide; acetonitrile / 1 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(II) methyl-t-butyl ether adduct / toluene / 8 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(II) methyl-t-butyl ether adduct; XPhos; In N,N-dimethyl-formamide; toluene; acetonitrile;