2-chloro-N-[5-[(dimethyl-tert-butyl-silyl)oxymethyl]-2-methyl-phenyl]-N-methyl-pyrimidin-4-amine

Base Information

Chemical Name:2-chloro-N-[5-[(dimethyl-tert-butyl-silyl)oxymethyl]-2-methyl-phenyl]-N-methyl-pyrimidin-4-amine
CAS No.:1075215-77-8
Molecular Formula:C₁₉H₂₈ClN₃OSi
Molecular Weight:377.989
Hs Code.:

Synonyms:2-chloro-N-[5-[(dimethyl-tert-butyl-silyl)oxymethyl]-2-methyl-phenyl]-N-methyl-pyrimidin-4-amine

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Chemical Property of 2-chloro-N-[5-[(dimethyl-tert-butyl-silyl)oxymethyl]-2-methyl-phenyl]-N-methyl-pyrimidin-4-amine

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Technology Process of 2-chloro-N-[5-[(dimethyl-tert-butyl-silyl)oxymethyl]-2-methyl-phenyl]-N-methyl-pyrimidin-4-amine

There total 3 articles about 2-chloro-N-[5-[(dimethyl-tert-butyl-silyl)oxymethyl]-2-methyl-phenyl]-N-methyl-pyrimidin-4-amine 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: 100.0%

: 1075215-76-7
2-chloro-N-[5-[(dimethyl-tert-butyl-silyl)oxymethyl]-2-methyl-phenyl]pyrimidin-4-amine

: 74-88-4
methyl iodide

: 1075215-77-8
2-chloro-N-[5-[(dimethyl-tert-butyl-silyl)oxymethyl]-2-methyl-phenyl]-N-methyl-pyrimidin-4-amine

Guidance literature:: With caesium carbonate; In acetonitrile; at 20 - 45 ℃; for 3h;

Reference yield:

: 1051899-86-5
[3-[(2-chloropyrimidin-4-yl)-methyl-amino]-4-methyl-phenyl]methanol

: 18162-48-6
tert-butyldimethylsilyl chloride

: 1075215-77-8
2-chloro-N-[5-[(dimethyl-tert-butyl-silyl)oxymethyl]-2-methyl-phenyl]-N-methyl-pyrimidin-4-amine

Guidance literature:: With 1H-imidazole; In N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2011.03.009

Reference yield:

: 81863-45-8
3-(hydroxymethyl)-6-methylaniline

: 1075215-77-8
2-chloro-N-[5-[(dimethyl-tert-butyl-silyl)oxymethyl]-2-methyl-phenyl]-N-methyl-pyrimidin-4-amine

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / ethanol / 18 h / Heating / reflux

2: 1H-imidazole / N,N-dimethyl-formamide / 16 h / 20 °C

3: caesium carbonate / acetonitrile / 3 h / 20 - 45 °C

With 1H-imidazole; caesium carbonate; triethylamine; In ethanol; N,N-dimethyl-formamide; acetonitrile;