N-benzyl-2-(3-(2,2-dimethoxyethyl)-3-(4-fluorobenzyl)ureido)-4-methylthiazole-5-carboxamide

Base Information

Chemical Name:N-benzyl-2-(3-(2,2-dimethoxyethyl)-3-(4-fluorobenzyl)ureido)-4-methylthiazole-5-carboxamide
CAS No.:1072806-38-2
Molecular Formula:C₂₄H₂₇FN₄O₄S
Molecular Weight:486.567
Hs Code.:

Synonyms:N-benzyl-2-(3-(2,2-dimethoxyethyl)-3-(4-fluorobenzyl)ureido)-4-methylthiazole-5-carboxamide

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Chemical Property of N-benzyl-2-(3-(2,2-dimethoxyethyl)-3-(4-fluorobenzyl)ureido)-4-methylthiazole-5-carboxamide

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Technology Process of N-benzyl-2-(3-(2,2-dimethoxyethyl)-3-(4-fluorobenzyl)ureido)-4-methylthiazole-5-carboxamide

There total 4 articles about N-benzyl-2-(3-(2,2-dimethoxyethyl)-3-(4-fluorobenzyl)ureido)-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: 77.0%

: 21709-39-7
2-amino-4-methylthiazole-5-carboxylic acid benzylamide

: 500782-63-8
2-(4-florobenzylamino)acetaldehyde dimethyl acetal

: 530-62-1
1,1'-carbonyldiimidazole

: 1072806-38-2
N-benzyl-2-(3-(2,2-dimethoxyethyl)-3-(4-fluorobenzyl)ureido)-4-methylthiazole-5-carboxamide

Guidance literature:: 2-amino-4-methylthiazole-5-carboxylic acid benzylamide; 1,1'-carbonyldiimidazole; In tetrahydrofuran; at 20 ℃; for 6h;

2-(4-florobenzylamino)acetaldehyde dimethyl acetal; In tetrahydrofuran; at 20 ℃; for 17h;

Reference yield:

: 140-75-0
para-fluorobenzylamine

: 1072806-38-2
N-benzyl-2-(3-(2,2-dimethoxyethyl)-3-(4-fluorobenzyl)ureido)-4-methylthiazole-5-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: water; sodium tris(acetoxy)borohydride / tetrahydrofuran / 5 - 12 h / 20 °C

2.1: tetrahydrofuran / 6 h / 20 °C

2.2: 17 h / 20 °C

With water; sodium tris(acetoxy)borohydride; In tetrahydrofuran;

Reference yield:

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

: 1072806-38-2
N-benzyl-2-(3-(2,2-dimethoxyethyl)-3-(4-fluorobenzyl)ureido)-4-methylthiazole-5-carboxamide

Guidance literature:: Multi-step reaction with 3 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 / 6 h / 20 °C

3.2: 17 h / 20 °C

With sodium hydroxide; water; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; N,N-dimethyl-formamide;