N-[4-[7-tert-butyl-5-(2,4-dioxopyrimidin-1-yl)-8-methoxy-2-quinolyl]phenyl]methanesulfonamide

Base Information

Chemical Name:N-[4-[7-tert-butyl-5-(2,4-dioxopyrimidin-1-yl)-8-methoxy-2-quinolyl]phenyl]methanesulfonamide
CAS No.:1246277-51-9
Molecular Formula:C₂₅H₂₆N₄O₅S
Molecular Weight:494.571
Hs Code.:

Synonyms:N-[4-[7-tert-butyl-5-(2,4-dioxopyrimidin-1-yl)-8-methoxy-2-quinolyl]phenyl]methanesulfonamide

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Chemical Property of N-[4-[7-tert-butyl-5-(2,4-dioxopyrimidin-1-yl)-8-methoxy-2-quinolyl]phenyl]methanesulfonamide

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Technology Process of N-[4-[7-tert-butyl-5-(2,4-dioxopyrimidin-1-yl)-8-methoxy-2-quinolyl]phenyl]methanesulfonamide

There total 6 articles about N-[4-[7-tert-butyl-5-(2,4-dioxopyrimidin-1-yl)-8-methoxy-2-quinolyl]phenyl]methanesulfonamide 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: 14.0%

: 1359946-45-4
N-[4-(5-bromo-7-tert-butyl-8-methoxy-2-quinolyl)phenyl]methanesulfonamide

: 66-22-8,144104-68-7,18324-22-6,27072-01-1,2920-92-5,51953-19-6
uracil

: 1246277-51-9
N-[4-[7-tert-butyl-5-(2,4-dioxopyrimidin-1-yl)-8-methoxy-2-quinolyl]phenyl]methanesulfonamide

Guidance literature:: With potassium phosphate; copper(l) iodide; N-(2-cyanophenyl)pyridine-2-carboxamide; In dimethyl sulfoxide; at 150 ℃; for 5h; Inert atmosphere; Microwave irradiation;
DOI:10.1021/jm401329s

Reference yield:

: 555-16-8
4-nitrobenzaldehdye

: 1246277-51-9
N-[4-[7-tert-butyl-5-(2,4-dioxopyrimidin-1-yl)-8-methoxy-2-quinolyl]phenyl]methanesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: acetonitrile / 0.75 h / 20 °C

1.2: 16 h

2.1: ammonium chloride / iron / water; methanol / 1.5 h / Reflux

3.1: pyridine / dichloromethane / 0.75 h / 0 °C

4.1: potassium phosphate; copper(l) iodide; pyridine-2-carboxylic acid (2-cyanophenyl)amide / dimethyl sulfoxide / 5 h / 150 °C / Sealed; Microwave irradiation

4.2: pH 2

With pyridine; potassium phosphate; copper(l) iodide; pyridine-2-carboxylic acid (2-cyanophenyl)amide; ammonium chloride; iron; In methanol; dichloromethane; water; dimethyl sulfoxide; acetonitrile;

Reference yield:

: 474554-51-3
5-bromo-3-tert-butyl-2-methoxyaniline

: 1246277-51-9
N-[4-[7-tert-butyl-5-(2,4-dioxopyrimidin-1-yl)-8-methoxy-2-quinolyl]phenyl]methanesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: acetonitrile / 0.75 h / 20 °C

1.2: 16 h

2.1: ammonium chloride / iron / water; methanol / 1.5 h / Reflux

3.1: pyridine / dichloromethane / 0.75 h / 0 °C

4.1: potassium phosphate; copper(l) iodide; pyridine-2-carboxylic acid (2-cyanophenyl)amide / dimethyl sulfoxide / 5 h / 150 °C / Sealed; Microwave irradiation

4.2: pH 2

With pyridine; potassium phosphate; copper(l) iodide; pyridine-2-carboxylic acid (2-cyanophenyl)amide; ammonium chloride; iron; In methanol; dichloromethane; water; dimethyl sulfoxide; acetonitrile;