4-fluoro-N-[1-(2-{2-[2-(2-{4-[2,4,6-trioxo-5-(4-phenoxyphenyl)hexahydropyrimidin-5-yl]piperazin-1-yl}ethoxy)ethoxy]ethoxy}ethyl)-1H-1,2,3-triazol-4-ylmethyl]benzenesulfonamide

Base Information

Chemical Name:4-fluoro-N-[1-(2-{2-[2-(2-{4-[2,4,6-trioxo-5-(4-phenoxyphenyl)hexahydropyrimidin-5-yl]piperazin-1-yl}ethoxy)ethoxy]ethoxy}ethyl)-1H-1,2,3-triazol-4-ylmethyl]benzenesulfonamide
CAS No.:1351556-91-6
Molecular Formula:C₃₇H₄₃FN₈O₉S
Molecular Weight:794.861
Hs Code.:

4-fluoro-N-[1-(2-{2-[2-(2-{4-[2,4,6-trioxo-5-(4-phenoxyphenyl)hexahydropyrimidin-5-yl]piperazin-1-yl}ethoxy)ethoxy]ethoxy}ethyl)-1H-1,2,3-triazol-4-ylmethyl]benzenesulfonamide

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Chemical Property of 4-fluoro-N-[1-(2-{2-[2-(2-{4-[2,4,6-trioxo-5-(4-phenoxyphenyl)hexahydropyrimidin-5-yl]piperazin-1-yl}ethoxy)ethoxy]ethoxy}ethyl)-1H-1,2,3-triazol-4-ylmethyl]benzenesulfonamide

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Technology Process of 4-fluoro-N-[1-(2-{2-[2-(2-{4-[2,4,6-trioxo-5-(4-phenoxyphenyl)hexahydropyrimidin-5-yl]piperazin-1-yl}ethoxy)ethoxy]ethoxy}ethyl)-1H-1,2,3-triazol-4-ylmethyl]benzenesulfonamide

There total 3 articles about 4-fluoro-N-[1-(2-{2-[2-(2-{4-[2,4,6-trioxo-5-(4-phenoxyphenyl)hexahydropyrimidin-5-yl]piperazin-1-yl}ethoxy)ethoxy]ethoxy}ethyl)-1H-1,2,3-triazol-4-ylmethyl]benzenesulfonamide 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: 27.0%

: 1024017-21-7
C₂₈H₃₅N₇O₇

: 321707-24-8
4-fluoro-N-(prop-2-yn-1-yl)benzenesulfonamide

: 1351556-91-6
4-fluoro-N-[1-(2-{2-[2-(2-{4-[2,4,6-trioxo-5-(4-phenoxyphenyl)hexahydropyrimidin-5-yl]piperazin-1-yl}ethoxy)ethoxy]ethoxy}ethyl)-1H-1,2,3-triazol-4-ylmethyl]benzenesulfonamide

Guidance literature:: With copper(ll) sulfate pentahydrate; sodium L-ascorbate; In water; N,N-dimethyl-formamide; at 20 ℃; for 18h;
DOI:10.1021/jm201142w

Reference yield:

: 5-bromo-5-(4-phenoxyphenyl)pyrimidine-2,4,6(1H,3H,5H)-trione

: 1351556-91-6
4-fluoro-N-[1-(2-{2-[2-(2-{4-[2,4,6-trioxo-5-(4-phenoxyphenyl)hexahydropyrimidin-5-yl]piperazin-1-yl}ethoxy)ethoxy]ethoxy}ethyl)-1H-1,2,3-triazol-4-ylmethyl]benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / N,N-dimethyl-formamide / 5 - 20 °C

2: copper(ll) sulfate pentahydrate; sodium L-ascorbate / water; N,N-dimethyl-formamide / 18 h / 20 °C

With copper(ll) sulfate pentahydrate; potassium carbonate; sodium L-ascorbate; In water; N,N-dimethyl-formamide;
DOI:10.1021/jm201142w

Reference yield:

: 219311-20-3
5-(4-phenoxyphenyl)pyrimidine-2,4,6-trione

: 1351556-91-6
4-fluoro-N-[1-(2-{2-[2-(2-{4-[2,4,6-trioxo-5-(4-phenoxyphenyl)hexahydropyrimidin-5-yl]piperazin-1-yl}ethoxy)ethoxy]ethoxy}ethyl)-1H-1,2,3-triazol-4-ylmethyl]benzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: N-Bromosuccinimide / N,N-dimethyl-formamide / 0.33 h / 5 - 10 °C

2: potassium carbonate / N,N-dimethyl-formamide / 5 - 20 °C

3: copper(ll) sulfate pentahydrate; sodium L-ascorbate / water; N,N-dimethyl-formamide / 18 h / 20 °C

With N-Bromosuccinimide; copper(ll) sulfate pentahydrate; potassium carbonate; sodium L-ascorbate; In water; N,N-dimethyl-formamide;
DOI:10.1021/jm201142w