tert-butyl [4-((3-((4-(4-fluoro-2-methoxyphenyl)-1,3,5-triazin-2-yl)amino)phenyl)methylsulfonamido)butyl]carbamate

Base Information

Chemical Name:tert-butyl [4-((3-((4-(4-fluoro-2-methoxyphenyl)-1,3,5-triazin-2-yl)amino)phenyl)methylsulfonamido)butyl]carbamate
CAS No.:1335491-07-0
Molecular Formula:C₂₆H₃₃FN₆O₅S
Molecular Weight:560.65
Hs Code.:

Synonyms:tert-butyl [4-((3-((4-(4-fluoro-2-methoxyphenyl)-1,3,5-triazin-2-yl)amino)phenyl)methylsulfonamido)butyl]carbamate

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Chemical Property of tert-butyl [4-((3-((4-(4-fluoro-2-methoxyphenyl)-1,3,5-triazin-2-yl)amino)phenyl)methylsulfonamido)butyl]carbamate

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Technology Process of tert-butyl [4-((3-((4-(4-fluoro-2-methoxyphenyl)-1,3,5-triazin-2-yl)amino)phenyl)methylsulfonamido)butyl]carbamate

There total 5 articles about tert-butyl [4-((3-((4-(4-fluoro-2-methoxyphenyl)-1,3,5-triazin-2-yl)amino)phenyl)methylsulfonamido)butyl]carbamate 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:

: 1335490-27-1
tert-butyl [4-(((3-((4-chloro-1,3,5-triazin-2-yl)amino)phenyl)methyl)sulfonamido)butyl]carbamate

: 179899-07-1
4-fluoro-2-methoxyphenylboronic acid

: 1335491-07-0
tert-butyl [4-((3-((4-(4-fluoro-2-methoxyphenyl)-1,3,5-triazin-2-yl)amino)phenyl)methylsulfonamido)butyl]carbamate

Guidance literature:: With potassium phosphate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In 1,4-dioxane; water; at 140 ℃; Inert atmosphere;

Reference yield:

: 58032-84-1
(3-nitrophenyl)methanesulfonyl chloride

: 1335491-07-0
tert-butyl [4-((3-((4-(4-fluoro-2-methoxyphenyl)-1,3,5-triazin-2-yl)amino)phenyl)methylsulfonamido)butyl]carbamate

Guidance literature:: Multi-step reaction with 4 steps

1: pyridine / dichloromethane / 5.5 h / 20 °C

2: hydrogen / Raney-Ni / methanol / 36 h / 50 °C / 3750.38 Torr / Parr reactor

3: N-ethyl-N,N-diisopropylamine / isopropyl alcohol; tetrahydrofuran / 0.5 h / -20 °C

4: potassium phosphate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,4-dioxane; water / 140 °C / Inert atmosphere

With pyridine; potassium phosphate; hydrogen; N-ethyl-N,N-diisopropylamine; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; water; isopropyl alcohol;

Reference yield:

: 68076-36-8
1-amino-4-[(tert-butyloxycarbonyl)amino]butane

: 1335491-07-0
tert-butyl [4-((3-((4-(4-fluoro-2-methoxyphenyl)-1,3,5-triazin-2-yl)amino)phenyl)methylsulfonamido)butyl]carbamate

Guidance literature:: Multi-step reaction with 4 steps

1: pyridine / dichloromethane / 5.5 h / 20 °C

2: hydrogen / Raney-Ni / methanol / 36 h / 50 °C / 3750.38 Torr / Parr reactor

3: N-ethyl-N,N-diisopropylamine / isopropyl alcohol; tetrahydrofuran / 0.5 h / -20 °C

4: potassium phosphate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,4-dioxane; water / 140 °C / Inert atmosphere

With pyridine; potassium phosphate; hydrogen; N-ethyl-N,N-diisopropylamine; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; water; isopropyl alcohol;