tert-butyl (2-((2-chloro-5-(trifluoromethyl)pyrimidin-4-yl)amino)phenyl)carbamate

Base Information

Chemical Name:tert-butyl (2-((2-chloro-5-(trifluoromethyl)pyrimidin-4-yl)amino)phenyl)carbamate
CAS No.:1622003-24-0
Molecular Formula:C₁₆H₁₆ClF₃N₄O₂
Molecular Weight:388.777
Hs Code.:

Synonyms:tert-butyl (2-((2-chloro-5-(trifluoromethyl)pyrimidin-4-yl)amino)phenyl)carbamate

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Chemical Property of tert-butyl (2-((2-chloro-5-(trifluoromethyl)pyrimidin-4-yl)amino)phenyl)carbamate

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Technology Process of tert-butyl (2-((2-chloro-5-(trifluoromethyl)pyrimidin-4-yl)amino)phenyl)carbamate

There total 1 articles about tert-butyl (2-((2-chloro-5-(trifluoromethyl)pyrimidin-4-yl)amino)phenyl)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: 35.2%

: 3932-97-6
2,4-dichloro-5-trifluoromethylpyrimidine

: 146651-75-4
tert–butyl (2–aminophenyl)carbamate

: 1622003-24-0
tert-butyl (2-((2-chloro-5-(trifluoromethyl)pyrimidin-4-yl)amino)phenyl)carbamate

: 1622003-43-3
tert-butyl(2-((4-chloro-5-(trifluoromethyl)pyrimidin-2-yl)amino)phenyl)carbamate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In ethanol; at 25 - 78 ℃; for 18h; Inert atmosphere;
DOI:10.1021/acs.jmedchem.5b00466

Reference yield:

: 1622003-24-0
tert-butyl (2-((2-chloro-5-(trifluoromethyl)pyrimidin-4-yl)amino)phenyl)carbamate

: N-(2-((2-((tetrahydro-2H-pyran-4-yl)amino)-5-(trifluoromethyl)pyrimidin-4-yl)amino)phenyl)acrylamide

Guidance literature:: Multi-step reaction with 3 steps

1: trifluoroacetic acid / dichloromethane / 18 h / 20 °C / Inert atmosphere

2: N-ethyl-N,N-diisopropylamine / 1-methyl-pyrrolidin-2-one / 0.83 h / 170 °C / Microwave irradiation

3: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 18 h / 5 - 22 °C / Inert atmosphere

With N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In 1-methyl-pyrrolidin-2-one; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/acs.jmedchem.5b00466

Reference yield:

: 1622003-24-0
tert-butyl (2-((2-chloro-5-(trifluoromethyl)pyrimidin-4-yl)amino)phenyl)carbamate

: N₄-(2-aminophenyl)-N₂-(tetrahydro-2H-pyran-4-yl)-5-(trifluoromethyl)pyrimidine-2,4-diamine

Guidance literature:: Multi-step reaction with 2 steps

1: trifluoroacetic acid / dichloromethane / 18 h / 20 °C / Inert atmosphere

2: N-ethyl-N,N-diisopropylamine / 1-methyl-pyrrolidin-2-one / 0.83 h / 170 °C / Microwave irradiation

With N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In 1-methyl-pyrrolidin-2-one; dichloromethane;
DOI:10.1021/acs.jmedchem.5b00466