ethyl ({5-[5-({[3-(1-cyano-1-methylethyl)phenyl]carbonyl}amino)-2-methylphenoxy]pyridin-2-yl}carbamothioyl)carbamate

Base Information

Chemical Name:ethyl ({5-[5-({[3-(1-cyano-1-methylethyl)phenyl]carbonyl}amino)-2-methylphenoxy]pyridin-2-yl}carbamothioyl)carbamate
CAS No.:1092395-12-4
Molecular Formula:C₂₇H₂₇N₅O₄S
Molecular Weight:517.608
Hs Code.:

Synonyms:ethyl ({5-[5-({[3-(1-cyano-1-methylethyl)phenyl]carbonyl}amino)-2-methylphenoxy]pyridin-2-yl}carbamothioyl)carbamate

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Chemical Property of ethyl ({5-[5-({[3-(1-cyano-1-methylethyl)phenyl]carbonyl}amino)-2-methylphenoxy]pyridin-2-yl}carbamothioyl)carbamate

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Technology Process of ethyl ({5-[5-({[3-(1-cyano-1-methylethyl)phenyl]carbonyl}amino)-2-methylphenoxy]pyridin-2-yl}carbamothioyl)carbamate

There total 5 articles about ethyl ({5-[5-({[3-(1-cyano-1-methylethyl)phenyl]carbonyl}amino)-2-methylphenoxy]pyridin-2-yl}carbamothioyl)carbamate 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:

: 1092395-10-2
N-{3-[(6-aminopyridin-3-yl)oxy]-4-methylphenyl}-3-(1-cyano-1-methylethyl)benzamide

: 16182-04-0
Ethoxycarbonyl isothiocyanate

: 1092395-12-4
ethyl ({5-[5-({[3-(1-cyano-1-methylethyl)phenyl]carbonyl}amino)-2-methylphenoxy]pyridin-2-yl}carbamothioyl)carbamate

Guidance literature:: In dimethyl sulfoxide; at 20 ℃; for 6h;

Reference yield:

: 1092395-14-6
3-(1-cyanocyclopropyl)benzoyl chloride

: 1092395-12-4
ethyl ({5-[5-({[3-(1-cyano-1-methylethyl)phenyl]carbonyl}amino)-2-methylphenoxy]pyridin-2-yl}carbamothioyl)carbamate

Guidance literature:: Multi-step reaction with 4 steps

1: sodium hydrogencarbonate / tetrahydrofuran; water / 5 h / 20 °C

2: caesium carbonate / N,N-dimethyl-formamide / 4 h / 60 °C

3: hydrogen / palladium 10% on activated carbon / methanol / 16 h / 20 °C / 1520.1 Torr

4: dimethyl sulfoxide / 6 h / 20 °C

With hydrogen; sodium hydrogencarbonate; caesium carbonate; palladium 10% on activated carbon; In tetrahydrofuran; methanol; water; dimethyl sulfoxide; N,N-dimethyl-formamide;

Reference yield:

: 1092395-08-8
3-(1-cyano-1-methylethyl)-N-(3-hydroxy-4-methylphenyl)benzamide

: 1092395-12-4
ethyl ({5-[5-({[3-(1-cyano-1-methylethyl)phenyl]carbonyl}amino)-2-methylphenoxy]pyridin-2-yl}carbamothioyl)carbamate

Guidance literature:: Multi-step reaction with 3 steps

1: caesium carbonate / N,N-dimethyl-formamide / 4 h / 60 °C

2: hydrogen / palladium 10% on activated carbon / methanol / 16 h / 20 °C / 1520.1 Torr

3: dimethyl sulfoxide / 6 h / 20 °C

With hydrogen; caesium carbonate; palladium 10% on activated carbon; In methanol; dimethyl sulfoxide; N,N-dimethyl-formamide;