N-(4-fluoro-2-(1,1-dioxo-1λ6-[1,2]thiazinan-2-yl)benzylcarbamoyl)-5-hydroxy-1-methyl-6-oxo-2-(tetrahydrofuran-3-yl)-1,6-dihydropyrimidine-4-carboxamide

Base Information

Chemical Name:N-(4-fluoro-2-(1,1-dioxo-1λ6-[1,2]thiazinan-2-yl)benzylcarbamoyl)-5-hydroxy-1-methyl-6-oxo-2-(tetrahydrofuran-3-yl)-1,6-dihydropyrimidine-4-carboxamide
CAS No.:1092544-77-8
Molecular Formula:C₂₁H₂₅FN₄O₆S
Molecular Weight:480.517
Hs Code.:

N-(4-fluoro-2-(1,1-dioxo-1λ6-[1,2]thiazinan-2-yl)benzylcarbamoyl)-5-hydroxy-1-methyl-6-oxo-2-(tetrahydrofuran-3-yl)-1,6-dihydropyrimidine-4-carboxamide

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Chemical Property of N-(4-fluoro-2-(1,1-dioxo-1λ6-[1,2]thiazinan-2-yl)benzylcarbamoyl)-5-hydroxy-1-methyl-6-oxo-2-(tetrahydrofuran-3-yl)-1,6-dihydropyrimidine-4-carboxamide

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Technology Process of N-(4-fluoro-2-(1,1-dioxo-1λ6-[1,2]thiazinan-2-yl)benzylcarbamoyl)-5-hydroxy-1-methyl-6-oxo-2-(tetrahydrofuran-3-yl)-1,6-dihydropyrimidine-4-carboxamide

There total 5 articles about N-(4-fluoro-2-(1,1-dioxo-1λ6-[1,2]thiazinan-2-yl)benzylcarbamoyl)-5-hydroxy-1-methyl-6-oxo-2-(tetrahydrofuran-3-yl)-1,6-dihydropyrimidine-4-carboxamide 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: 51.0%

: 1092544-77-8
N-(4-fluoro-2-(1,1-dioxo-1λ6-[1,2]thiazinan-2-yl)benzylcarbamoyl)-5-hydroxy-1-methyl-6-oxo-2-(tetrahydrofuran-3-yl)-1,6-dihydropyrimidine-4-carboxamide

Guidance literature:

Reference yield:

: 14631-44-8
3-cyanotetrahydrofuran

: 1092544-77-8
N-(4-fluoro-2-(1,1-dioxo-1λ6-[1,2]thiazinan-2-yl)benzylcarbamoyl)-5-hydroxy-1-methyl-6-oxo-2-(tetrahydrofuran-3-yl)-1,6-dihydropyrimidine-4-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: sodium carbonate / ethanol; N,N-dimethyl-formamide / 80 °C

2: ethanol; N,N-dimethyl-formamide / 20 °C

3: 5,5-dimethyl-1,3-cyclohexadiene / Pyrolysis

4: triethylamine / ethanol; N,N-dimethyl-formamide / Heating

With sodium carbonate; triethylamine; In 5,5-dimethyl-1,3-cyclohexadiene; ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2014.11.060

Reference yield:

: C₆H₁₂N₂O₂

: 1092544-77-8
N-(4-fluoro-2-(1,1-dioxo-1λ6-[1,2]thiazinan-2-yl)benzylcarbamoyl)-5-hydroxy-1-methyl-6-oxo-2-(tetrahydrofuran-3-yl)-1,6-dihydropyrimidine-4-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: ethanol; N,N-dimethyl-formamide / 20 °C

2: 5,5-dimethyl-1,3-cyclohexadiene / Pyrolysis

3: triethylamine / ethanol; N,N-dimethyl-formamide / Heating

With triethylamine; In 5,5-dimethyl-1,3-cyclohexadiene; ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2014.11.060