[5-(2-Chloro-phenyl)-2-methylsulfanyl-pyrimidin-4-yl]-methyl-carbamic acid tert.-butyl ester

Base Information

Chemical Name:[5-(2-Chloro-phenyl)-2-methylsulfanyl-pyrimidin-4-yl]-methyl-carbamic acid tert.-butyl ester
CAS No.:311335-87-2
Molecular Formula:C₁₇H₂₀ClN₃O₂S
Molecular Weight:365.884
Hs Code.:

Synonyms:[5-(2-Chloro-phenyl)-2-methylsulfanyl-pyrimidin-4-yl]-methyl-carbamic acid tert.-butyl ester

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Chemical Property of [5-(2-Chloro-phenyl)-2-methylsulfanyl-pyrimidin-4-yl]-methyl-carbamic acid tert.-butyl ester

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Technology Process of [5-(2-Chloro-phenyl)-2-methylsulfanyl-pyrimidin-4-yl]-methyl-carbamic acid tert.-butyl ester

There total 5 articles about [5-(2-Chloro-phenyl)-2-methylsulfanyl-pyrimidin-4-yl]-methyl-carbamic acid tert.-butyl ester 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: 96.0%

: 311335-86-1
[5-(2-Chloro-phenyl)-2-methylsulfanyl-pyrimidin-4-yl]-carbamic acid tert.-butyl ester

: 74-88-4
methyl iodide

: 311335-87-2
[5-(2-Chloro-phenyl)-2-methylsulfanyl-pyrimidin-4-yl]-methyl-carbamic acid tert.-butyl ester

Guidance literature:: [5-(2-Chloro-phenyl)-2-methylsulfanyl-pyrimidin-4-yl]-carbamic acid tert.-butyl ester; With sodium hydride; In N,N-dimethyl-formamide; for 1h;

methyl iodide; In DMF (N,N-dimethyl-formamide); at 0 ℃; for 3h;

Reference yield:

: 3900-89-8
2-Chlorobenzeneboronic acid

: 311335-87-2
[5-(2-Chloro-phenyl)-2-methylsulfanyl-pyrimidin-4-yl]-methyl-carbamic acid tert.-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine / palladium diacetate; triphenylphosphine / N,N-dimethyl-formamide / 4 h / 105 °C

2.1: sodium hydroxide / ethanol / 1 h / 20 °C

2.2: pH 1

3.1: diphenylphosphoranyl azide; triethylamine / tetrahydrofuran / 12 h

4.1: sodium hydride / N,N-dimethyl-formamide / 1 h

4.2: 3 h / 0 °C

With sodium hydroxide; diphenylphosphoranyl azide; sodium hydride; triethylamine; palladium diacetate; triphenylphosphine; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide;

Reference yield:

: 74840-38-3
ethyl 5-bromo-2-methylthio-4-pyrimidinecarboxylate

: 311335-87-2
[5-(2-Chloro-phenyl)-2-methylsulfanyl-pyrimidin-4-yl]-methyl-carbamic acid tert.-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine / palladium diacetate; triphenylphosphine / N,N-dimethyl-formamide / 4 h / 105 °C

2.1: sodium hydroxide / ethanol / 1 h / 20 °C

2.2: pH 1

3.1: diphenylphosphoranyl azide; triethylamine / tetrahydrofuran / 12 h

4.1: sodium hydride / N,N-dimethyl-formamide / 1 h

4.2: 3 h / 0 °C

With sodium hydroxide; diphenylphosphoranyl azide; sodium hydride; triethylamine; palladium diacetate; triphenylphosphine; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide;