{1-[N-(5-bromo-1,3-dimethyl-2,6-dioxo-1,2,3,6-tetrahydro-pyrimidin-4-yl)-carbamimidoyl]-piperidin-3-yl}-carbamic acid tert-butyl ester

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Chemical Name:{1-[N-(5-bromo-1,3-dimethyl-2,6-dioxo-1,2,3,6-tetrahydro-pyrimidin-4-yl)-carbamimidoyl]-piperidin-3-yl}-carbamic acid tert-butyl ester
CAS No.:851608-41-8
Molecular Formula:C₁₇H₂₇BrN₆O₄
Molecular Weight:459.343
Hs Code.:

Synonyms:{1-[N-(5-bromo-1,3-dimethyl-2,6-dioxo-1,2,3,6-tetrahydro-pyrimidin-4-yl)-carbamimidoyl]-piperidin-3-yl}-carbamic acid tert-butyl ester

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Chemical Property of {1-[N-(5-bromo-1,3-dimethyl-2,6-dioxo-1,2,3,6-tetrahydro-pyrimidin-4-yl)-carbamimidoyl]-piperidin-3-yl}-carbamic acid tert-butyl ester

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Technology Process of {1-[N-(5-bromo-1,3-dimethyl-2,6-dioxo-1,2,3,6-tetrahydro-pyrimidin-4-yl)-carbamimidoyl]-piperidin-3-yl}-carbamic acid tert-butyl ester

There total 1 articles about {1-[N-(5-bromo-1,3-dimethyl-2,6-dioxo-1,2,3,6-tetrahydro-pyrimidin-4-yl)-carbamimidoyl]-piperidin-3-yl}-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:

: 184637-48-7,172603-05-3
t-butyl piperidin-3-ylcarbamate

: 851608-41-8
{1-[N-(5-bromo-1,3-dimethyl-2,6-dioxo-1,2,3,6-tetrahydro-pyrimidin-4-yl)-carbamimidoyl]-piperidin-3-yl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 93 percent / N,N-diisorpopylethylamine / dimethylformamide / 96 h / 20 °C

2: 62 percent / KOEt / ethanol / 1.5 h / Heating

With potassium ethoxide; N-ethyl-N,N-diisopropylamine; In ethanol; N,N-dimethyl-formamide;
DOI:10.1021/ol0504751

Reference yield:

: 851608-41-8
{1-[N-(5-bromo-1,3-dimethyl-2,6-dioxo-1,2,3,6-tetrahydro-pyrimidin-4-yl)-carbamimidoyl]-piperidin-3-yl}-carbamic acid tert-butyl ester

: 2-(8-(3-Aminopiperidin-1-yl)-1,3-dimethyl-2,6-dioxo-1,2,3,6-tetrahydropurin-7-ylmethyl)benzonitrile

Guidance literature:: Multi-step reaction with 3 steps

1: 77 percent / NaH; CuI / tetrahydrofuran / 75 °C

2: 50 percent / K₂CO₃ / dimethylformamide / 23 °C

3: TFA / CH₂Cl₂ / 23 °C

With copper(l) iodide; sodium hydride; potassium carbonate; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2006.09.024

Reference yield:

: 851608-41-8
{1-[N-(5-bromo-1,3-dimethyl-2,6-dioxo-1,2,3,6-tetrahydro-pyrimidin-4-yl)-carbamimidoyl]-piperidin-3-yl}-carbamic acid tert-butyl ester

: 918931-51-8
{1-[7-(2-cyano-benzyl)-1,3-dimethyl-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-8-yl]-piperidin-3-yl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 77 percent / NaH; CuI / tetrahydrofuran / 75 °C

2: 50 percent / K₂CO₃ / dimethylformamide / 23 °C

With copper(l) iodide; sodium hydride; potassium carbonate; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2006.09.024