1-{[2-isopropoxy-6-(trifluoromethyl)pyridin-3-yl]methyl}-3-{4-[(sulfamoylamino)methyl]phenyl}urea

Base Information

Chemical Name:1-{[2-isopropoxy-6-(trifluoromethyl)pyridin-3-yl]methyl}-3-{4-[(sulfamoylamino)methyl]phenyl}urea
CAS No.:1428745-24-7
Molecular Formula:C₁₈H₂₂F₃N₅O₄S
Molecular Weight:461.465
Hs Code.:

Synonyms:1-{[2-isopropoxy-6-(trifluoromethyl)pyridin-3-yl]methyl}-3-{4-[(sulfamoylamino)methyl]phenyl}urea

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Chemical Property of 1-{[2-isopropoxy-6-(trifluoromethyl)pyridin-3-yl]methyl}-3-{4-[(sulfamoylamino)methyl]phenyl}urea

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Technology Process of 1-{[2-isopropoxy-6-(trifluoromethyl)pyridin-3-yl]methyl}-3-{4-[(sulfamoylamino)methyl]phenyl}urea

There total 8 articles about 1-{[2-isopropoxy-6-(trifluoromethyl)pyridin-3-yl]methyl}-3-{4-[(sulfamoylamino)methyl]phenyl}urea 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: 66.0%

: 1428745-53-2
tert-butyl N-(4-(3-((2-isopropoxy-6-(trifluoromethyl)pyridin-3-yl)methyl)ureido)benzyl)sulfamoylcarbamate

: 1428745-24-7
1-{[2-isopropoxy-6-(trifluoromethyl)pyridin-3-yl]methyl}-3-{4-[(sulfamoylamino)methyl]phenyl}urea

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 0 - 20 ℃; for 2.5h;

Reference yield:

: 99-99-0
1-methyl-4-nitrobenzene

: 1428745-24-7
1-{[2-isopropoxy-6-(trifluoromethyl)pyridin-3-yl]methyl}-3-{4-[(sulfamoylamino)methyl]phenyl}urea

Guidance literature:: Multi-step reaction with 8 steps

1.1: N-Bromosuccinimide; dibenzoyl peroxide / tetrachloromethane / 24 h / Reflux

2.1: N,N-dimethyl-formamide

3.1: hydrazine hydrate / tetrahydrofuran / 6 h / Reflux

4.1: dichloromethane / 0.17 h

4.2: 0.5 h / 50 °C

4.3: 3 h / 20 °C

5.1: hydrogen; palladium 10% on activated carbon / tetrahydrofuran; ethanol / 6 h / 20 °C

6.1: pyridine / tetrahydrofuran; acetonitrile / 1 h / 0 - 20 °C

7.1: dmap / acetonitrile / 50 °C

8.1: trifluoroacetic acid / dichloromethane / 2.5 h / 0 - 20 °C

With pyridine; dmap; N-Bromosuccinimide; palladium 10% on activated carbon; hydrogen; hydrazine hydrate; trifluoroacetic acid; dibenzoyl peroxide; In tetrahydrofuran; tetrachloromethane; ethanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 1402586-16-6
N-[4-[[(tert-butoxycarbonyl-sulfamoyl)amino]-methyl]-phenyl]-carbamic acid phenyl ester

: 1428745-24-7
1-{[2-isopropoxy-6-(trifluoromethyl)pyridin-3-yl]methyl}-3-{4-[(sulfamoylamino)methyl]phenyl}urea

Guidance literature:: Multi-step reaction with 2 steps

1: dmap / acetonitrile / 50 °C

2: trifluoroacetic acid / dichloromethane / 2.5 h / 0 - 20 °C

With dmap; trifluoroacetic acid; In dichloromethane; acetonitrile;