N-benzyl-2-(3-(4-fluorophenyl)-2,5-dioxoimidazolidin-1-yl)-4-methylthiazole-5-carboxamide

Base Information

Chemical Name:N-benzyl-2-(3-(4-fluorophenyl)-2,5-dioxoimidazolidin-1-yl)-4-methylthiazole-5-carboxamide
CAS No.:1072802-22-2
Molecular Formula:C₂₁H₁₇FN₄O₃S
Molecular Weight:424.455
Hs Code.:

Synonyms:N-benzyl-2-(3-(4-fluorophenyl)-2,5-dioxoimidazolidin-1-yl)-4-methylthiazole-5-carboxamide

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Chemical Property of N-benzyl-2-(3-(4-fluorophenyl)-2,5-dioxoimidazolidin-1-yl)-4-methylthiazole-5-carboxamide

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Technology Process of N-benzyl-2-(3-(4-fluorophenyl)-2,5-dioxoimidazolidin-1-yl)-4-methylthiazole-5-carboxamide

There total 6 articles about N-benzyl-2-(3-(4-fluorophenyl)-2,5-dioxoimidazolidin-1-yl)-4-methylthiazole-5-carboxamide 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: 18.0%

: 1072802-21-1
N-benzyl-2-(3-(4-fluorophenyl)-5-hydroxy-2-oxoimidazolidin-1-yl)-4-methylthiazole-5-carboxamide

: 1072802-22-2
N-benzyl-2-(3-(4-fluorophenyl)-2,5-dioxoimidazolidin-1-yl)-4-methylthiazole-5-carboxamide

Guidance literature:: With tetrapropylammonium perruthennate; 4-methylmorpholine N-oxide; In chloroform; at 20 ℃; for 1h;

Reference yield:

: 7210-76-6
ethyl-2-amino-4-methylthiazole-5-carboxylate

: 1072802-22-2
N-benzyl-2-(3-(4-fluorophenyl)-2,5-dioxoimidazolidin-1-yl)-4-methylthiazole-5-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydroxide; water / tetrahydrofuran / 18 h / Heating / reflux

1.2: pH 5 - 6

2.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 0.5 h

2.2: 48 h / 20 °C

3.1: tetrahydrofuran / 11 h / 20 °C

3.2: 17 h / 20 °C

4.1: sulfuric acid; water / tetrahydrofuran / 53 h / 20 °C

5.1: tetrapropylammonium perruthennate; 4-methylmorpholine N-oxide / chloroform / 1 h / 20 °C

With sodium hydroxide; tetrapropylammonium perruthennate; sulfuric acid; water; 4-methylmorpholine N-oxide; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; chloroform; N,N-dimethyl-formamide;

Reference yield:

: 67899-00-7
2-amino-4-methyl-thiazole-5-carboxylic acid

: 1072802-22-2
N-benzyl-2-(3-(4-fluorophenyl)-2,5-dioxoimidazolidin-1-yl)-4-methylthiazole-5-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 0.5 h

1.2: 48 h / 20 °C

2.1: tetrahydrofuran / 11 h / 20 °C

2.2: 17 h / 20 °C

3.1: sulfuric acid; water / tetrahydrofuran / 53 h / 20 °C

4.1: tetrapropylammonium perruthennate; 4-methylmorpholine N-oxide / chloroform / 1 h / 20 °C

With tetrapropylammonium perruthennate; sulfuric acid; water; 4-methylmorpholine N-oxide; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; chloroform; N,N-dimethyl-formamide;