N-(4-(3-((2-m-tolyl-6-(trifluoromethyl)pyridin-3-yl)methyl)ureido)benzyl)methanesulfonamide

Base Information

Chemical Name:N-(4-(3-((2-m-tolyl-6-(trifluoromethyl)pyridin-3-yl)methyl)ureido)benzyl)methanesulfonamide
CAS No.:1428764-17-3
Molecular Formula:C₂₃H₂₃F₃N₄O₃S
Molecular Weight:492.522
Hs Code.:

Synonyms:N-(4-(3-((2-m-tolyl-6-(trifluoromethyl)pyridin-3-yl)methyl)ureido)benzyl)methanesulfonamide

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Chemical Property of N-(4-(3-((2-m-tolyl-6-(trifluoromethyl)pyridin-3-yl)methyl)ureido)benzyl)methanesulfonamide

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Technology Process of N-(4-(3-((2-m-tolyl-6-(trifluoromethyl)pyridin-3-yl)methyl)ureido)benzyl)methanesulfonamide

There total 12 articles about N-(4-(3-((2-m-tolyl-6-(trifluoromethyl)pyridin-3-yl)methyl)ureido)benzyl)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: 63.0%

: 1428765-32-5
(2-m-tolyl-6-(trifluoromethyl)pyridin-3-yl)methanamine

: 1402586-09-7
phenyl 4-(methylsulfonamidomethyl)phenylcarbamate

: 1428764-17-3
N-(4-(3-((2-m-tolyl-6-(trifluoromethyl)pyridin-3-yl)methyl)ureido)benzyl)methanesulfonamide

Guidance literature:: With dmap; In acetonitrile; at 20 - 50 ℃; for 16h; Enzymatic reaction;

Reference yield:

: 619-73-8
4-nitrobenzyl chloride

: 1428764-17-3
N-(4-(3-((2-m-tolyl-6-(trifluoromethyl)pyridin-3-yl)methyl)ureido)benzyl)methanesulfonamide

Guidance literature:: Multi-step reaction with 7 steps

1: toluene / 4 h / 20 - 80 °C

2: N,N-dimethyl-formamide / 20 °C

3: hydrazine hydrate; toluene-4-sulfonic acid / tetrahydrofuran / 6 h / Reflux

4: pyridine / 1 h / 20 °C

5: palladium 10% on activated carbon; hydrogen / tetrahydrofuran; methanol / 20 °C

6: pyridine / tetrahydrofuran; acetonitrile / 3 h / 20 °C / Inert atmosphere

7: dmap / acetonitrile / 16 h / 20 - 50 °C

With pyridine; dmap; palladium 10% on activated carbon; hydrogen; toluene-4-sulfonic acid; hydrazine hydrate; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; toluene; acetonitrile;

Reference yield:

: 7409-30-5
p-nitrobenzylamine

: 1428764-17-3
N-(4-(3-((2-m-tolyl-6-(trifluoromethyl)pyridin-3-yl)methyl)ureido)benzyl)methanesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: pyridine / 1 h / 20 °C

2: palladium 10% on activated carbon; hydrogen / tetrahydrofuran; methanol / 20 °C

3: pyridine / tetrahydrofuran; acetonitrile / 3 h / 20 °C / Inert atmosphere

4: dmap / acetonitrile / 16 h / 20 - 50 °C

With pyridine; dmap; palladium 10% on activated carbon; hydrogen; In tetrahydrofuran; methanol; acetonitrile;