N-{4'-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}biphenyl-2-ylsulfonyl}propionamide

Base Information

Chemical Name:N-{4'-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}biphenyl-2-ylsulfonyl}propionamide
CAS No.:1268155-52-7
Molecular Formula:C₃₀H₃₃N₅O₅S
Molecular Weight:575.689
Hs Code.:

Synonyms:N-{4'-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}biphenyl-2-ylsulfonyl}propionamide

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Chemical Property of N-{4'-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}biphenyl-2-ylsulfonyl}propionamide

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Technology Process of N-{4'-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}biphenyl-2-ylsulfonyl}propionamide

There total 5 articles about N-{4'-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}biphenyl-2-ylsulfonyl}propionamide 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: 86.0%

: 1268155-79-8
4'-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}biphenyl-2-sulfonamide

: 79-03-8
propionyl chloride

: 1268155-52-7
N-{4'-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}biphenyl-2-ylsulfonyl}propionamide

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 15h; Inert atmosphere;

Reference yield:

: 1268155-77-6
5-(4-bromobenzyl)-6-butyl-3-(5-methoxypyrimidin-2-yl)-2-methylpyrimidin-4(3H)-one

: 1268155-52-7
N-{4'-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}biphenyl-2-ylsulfonyl}propionamide

Guidance literature:: Multi-step reaction with 3 steps

1: potassium phosphate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane / 4 h / Reflux; Inert atmosphere

2: trifluoroacetic acid / methoxybenzene / 24 h / 20 °C

3: triethylamine / dichloromethane / 15 h / 20 °C / Inert atmosphere

With potassium phosphate; triethylamine; trifluoroacetic acid; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1,4-dioxane; dichloromethane; methoxybenzene;

Reference yield:

: Methyl 2-[(4-bromophenyl)methyl]-3-oxoheptanoate

: 1268155-52-7
N-{4'-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}biphenyl-2-ylsulfonyl}propionamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: ammonium acetate; acetic acid / toluene / 10 h / Reflux

1.2: 4 h / 70 °C

2.1: trimethylaluminum / hexane; 1,2-dichloro-ethane / 1.33 h / 20 °C / Inert atmosphere

2.2: 20 °C / Reflux; Inert atmosphere

3.1: potassium phosphate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane / 4 h / Reflux; Inert atmosphere

4.1: trifluoroacetic acid / methoxybenzene / 24 h / 20 °C

5.1: triethylamine / dichloromethane / 15 h / 20 °C / Inert atmosphere

With potassium phosphate; ammonium acetate; trimethylaluminum; acetic acid; triethylamine; trifluoroacetic acid; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1,4-dioxane; hexane; dichloromethane; methoxybenzene; 1,2-dichloro-ethane; toluene;