N-[4-(2-{[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-methoxyphenyl]-amino}[1,2,4]triazolo[1,5-a]pyridin-6-yl)phenyl]-2-(4-fluorophenyl)-acetamide

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Chemical Name:N-[4-(2-{[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-methoxyphenyl]-amino}[1,2,4]triazolo[1,5-a]pyridin-6-yl)phenyl]-2-(4-fluorophenyl)-acetamide
CAS No.:1403330-18-6
Molecular Formula:C₃₄H₃₈FN₅O₃Si
Molecular Weight:611.791
Hs Code.:

Synonyms:N-[4-(2-{[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-methoxyphenyl]-amino}[1,2,4]triazolo[1,5-a]pyridin-6-yl)phenyl]-2-(4-fluorophenyl)-acetamide

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Chemical Property of N-[4-(2-{[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-methoxyphenyl]-amino}[1,2,4]triazolo[1,5-a]pyridin-6-yl)phenyl]-2-(4-fluorophenyl)-acetamide

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Technology Process of N-[4-(2-{[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-methoxyphenyl]-amino}[1,2,4]triazolo[1,5-a]pyridin-6-yl)phenyl]-2-(4-fluorophenyl)-acetamide

There total 2 articles about N-[4-(2-{[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-methoxyphenyl]-amino}[1,2,4]triazolo[1,5-a]pyridin-6-yl)phenyl]-2-(4-fluorophenyl)-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:

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

: 905103-73-3
[(4-bromo-3-methoxybenzyl)oxy](tert-butyl)dimethylsilane

: 1403330-18-6
N-[4-(2-{[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-methoxyphenyl]-amino}[1,2,4]triazolo[1,5-a]pyridin-6-yl)phenyl]-2-(4-fluorophenyl)-acetamide

Guidance literature:: With potassium phosphate; 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 1-methyl-pyrrolidin-2-one; toluene; for 2h; Inert atmosphere; Reflux;

Reference yield:

: 17100-64-0
(4-bromo-3-methoxyphenyl)methanol

: 1403330-18-6
N-[4-(2-{[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-methoxyphenyl]-amino}[1,2,4]triazolo[1,5-a]pyridin-6-yl)phenyl]-2-(4-fluorophenyl)-acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: 1H-imidazole; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 3 h / 20 °C

2: potassium phosphate / 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; 1-methyl-pyrrolidin-2-one / 2 h / Inert atmosphere; Reflux

With 1H-imidazole; potassium phosphate; N-ethyl-N,N-diisopropylamine; 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 tetrahydrofuran; 1-methyl-pyrrolidin-2-one; toluene;