tert-butyl 3-(4-((4-chloro-5-(trifluoromethyl)pyrimidin-2-yl)amino)phenyl)piperidine-1-carboxylate

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Chemical Name:tert-butyl 3-(4-((4-chloro-5-(trifluoromethyl)pyrimidin-2-yl)amino)phenyl)piperidine-1-carboxylate
CAS No.:1393900-90-7
Molecular Formula:C₂₁H₂₄ClF₃N₄O₂
Molecular Weight:456.895
Hs Code.:

Synonyms:tert-butyl 3-(4-((4-chloro-5-(trifluoromethyl)pyrimidin-2-yl)amino)phenyl)piperidine-1-carboxylate

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Chemical Property of tert-butyl 3-(4-((4-chloro-5-(trifluoromethyl)pyrimidin-2-yl)amino)phenyl)piperidine-1-carboxylate

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Technology Process of tert-butyl 3-(4-((4-chloro-5-(trifluoromethyl)pyrimidin-2-yl)amino)phenyl)piperidine-1-carboxylate

There total 4 articles about tert-butyl 3-(4-((4-chloro-5-(trifluoromethyl)pyrimidin-2-yl)amino)phenyl)piperidine-1-carboxylate 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: 90.0%

: 875798-79-1
3-(4-aminophenyl)piperidine-1-carboxylic acid tert-butyl ester

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

: 1393900-90-7
tert-butyl 3-(4-((4-chloro-5-(trifluoromethyl)pyrimidin-2-yl)amino)phenyl)piperidine-1-carboxylate

Guidance literature:: 2,4-dichloro-5-trifluoromethylpyrimidine; With zinc(II) chloride; In diethyl ether; 1,2-dichloro-ethane; tert-butyl alcohol; at 0 ℃; for 0.5h;

3-(4-aminophenyl)piperidine-1-carboxylic acid tert-butyl ester; In diethyl ether; 1,2-dichloro-ethane; tert-butyl alcohol; at 0 - 20 ℃; for 60h;

Reference yield:

: 1692-25-7
3-pyridylboronic acid

: 1393900-90-7
tert-butyl 3-(4-((4-chloro-5-(trifluoromethyl)pyrimidin-2-yl)amino)phenyl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: caesium carbonate / triphenylphosphine; palladium diacetate / N,N-dimethyl-formamide / 18 h / 80 °C

2.1: hydrogenchloride; hydrogen / water; methanol / 48 h / 2068.65 Torr / Inert atmosphere

2.2: 20 h / 20 °C

3.1: zinc(II) chloride / diethyl ether; 1,2-dichloro-ethane; tert-butyl alcohol / 0.5 h / 0 °C

3.2: 60 h / 0 - 20 °C

With hydrogenchloride; hydrogen; caesium carbonate; zinc(II) chloride; palladium diacetate; triphenylphosphine; In methanol; diethyl ether; water; 1,2-dichloro-ethane; N,N-dimethyl-formamide; tert-butyl alcohol;

Reference yield:

: 636-98-6
p-nitrobenzene iodide

: 1393900-90-7
tert-butyl 3-(4-((4-chloro-5-(trifluoromethyl)pyrimidin-2-yl)amino)phenyl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: caesium carbonate / triphenylphosphine; palladium diacetate / N,N-dimethyl-formamide / 18 h / 80 °C

2.1: hydrogenchloride; hydrogen / water; methanol / 48 h / 2068.65 Torr / Inert atmosphere

2.2: 20 h / 20 °C

3.1: zinc(II) chloride / diethyl ether; 1,2-dichloro-ethane; tert-butyl alcohol / 0.5 h / 0 °C

3.2: 60 h / 0 - 20 °C

With hydrogenchloride; hydrogen; caesium carbonate; zinc(II) chloride; palladium diacetate; triphenylphosphine; In methanol; diethyl ether; water; 1,2-dichloro-ethane; N,N-dimethyl-formamide; tert-butyl alcohol;