3-(1,3-dimethyl-10-(4-methylthiazol-2-yl)-2,4-dioxo-1,2,3,4,7,8,9,10-octahydropyrimido[4,5-a]indolizin-5-yl)benzonitrile

Base Information

• Chemical Name: 3-(1,3-dimethyl-10-(4-methylthiazol-2-yl)-2,4-dioxo-1,2,3,4,7,8,9,10-octahydropyrimido[4,5-a]indolizin-5-yl)benzonitrile
• CAS No.: 1614249-76-1
• Molecular Formula: C₂₃H₂₁N₅O₂S
• Molecular Weight: 431.518
• Mol file: 1614249-76-1.mol

Synonyms:3-(1,3-dimethyl-10-(4-methylthiazol-2-yl)-2,4-dioxo-1,2,3,4,7,8,9,10-octahydropyrimido[4,5-a]indolizin-5-yl)benzonitrile

Chemical Property of 3-(1,3-dimethyl-10-(4-methylthiazol-2-yl)-2,4-dioxo-1,2,3,4,7,8,9,10-octahydropyrimido[4,5-a]indolizin-5-yl)benzonitrile

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3-(1,3-dimethyl-10-(4-methylthiazol-2-yl)-2,4-dioxo-1,2,3,4,7,8,9,10-octahydropyrimido[4,5-a]indolizin-5-yl)benzonitrile

There total 12 articles about 3-(1,3-dimethyl-10-(4-methylthiazol-2-yl)-2,4-dioxo-1,2,3,4,7,8,9,10-octahydropyrimido[4,5-a]indolizin-5-yl)benzonitrile 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:

3-(1,3-dimethyl-10-(4-methylthiazol-2-yl)-2,4-dioxo-1,2,3,4,7,8-hexahydropyrimido[4,5-a]indolizin-5-yl)benzonitrile (1614251-47-6) → 3-(1,3-dimethyl-10-(4-methylthiazol-2-yl)-2,4-dioxo-1,2,3,4,7,8,9,10-octahydropyrimido[4,5-a]indolizin-5-yl)benzonitrile (1614249-76-1)

Guidance literature:

With palladium 10% on activated carbon; hydrogen; In tetrahydrofuran; ethanol; at 20 ℃; for 63h;

Reference yield:

1,3-dimethyl-2,4-dioxo-6-((2-(trimethylsilyl)ethoxy)methyl)-2,3,4,6-tetrahydro-1H-pyrrolo[3,4-d]pyrimidin-5-ylboronic acid (1613623-81-6) → 3-(1,3-dimethyl-10-(4-methylthiazol-2-yl)-2,4-dioxo-1,2,3,4,7,8,9,10-octahydropyrimido[4,5-a]indolizin-5-yl)benzonitrile (1614249-76-1)

Guidance literature:

Multi-step reaction with 9 steps

1.1: potassium carbonate / acetic acid butyl ester; water / 1.5 h / 80 °C

2.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 1 h / 60 °C

3.1: caesium carbonate / N,N-dimethyl-formamide / 2 h / 80 °C

4.1: lithium hydroxide; water / tetrahydrofuran / 4 h / 20 °C

4.2: pH 1

5.1: 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide / N,N-dimethyl-formamide / 12 h / 100 °C

6.1: 2,6-dimethylpyridine / dichloromethane / 2 h / Cooling with ice

7.1: triphenylphosphine; bis-triphenylphosphine-palladium(II) chloride; potassium phenolate / toluene / 3 h / 60 °C / Inert atmosphere

8.1: dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II); barium dihydroxide / acetonitrile; water / 1.75 h / 20 - 80 °C

9.1: hydrogen; palladium 10% on activated carbon / ethanol; tetrahydrofuran / 63 h / 20 °C

With 2,6-dimethylpyridine; bis-triphenylphosphine-palladium(II) chloride; barium dihydroxide; dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II); palladium 10% on activated carbon; potassium phenolate; tetrabutyl ammonium fluoride; water; hydrogen; potassium carbonate; caesium carbonate; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; triphenylphosphine; lithium hydroxide; In tetrahydrofuran; ethanol; dichloromethane; acetic acid butyl ester; water; N,N-dimethyl-formamide; toluene; acetonitrile;

Reference yield:

3-(1,3-dimethyl-2,4,10-trioxo-1,2,3,4,7,8,9,10-octahydropyrimido[4,5-a]indolizin-5-yl)benzonitrile (1614251-44-3) → 3-(1,3-dimethyl-10-(4-methylthiazol-2-yl)-2,4-dioxo-1,2,3,4,7,8,9,10-octahydropyrimido[4,5-a]indolizin-5-yl)benzonitrile (1614249-76-1)

Guidance literature:

Multi-step reaction with 4 steps

1: 2,6-dimethylpyridine / dichloromethane / 2 h / Cooling with ice

2: triphenylphosphine; bis-triphenylphosphine-palladium(II) chloride; potassium phenolate / toluene / 3 h / 60 °C / Inert atmosphere

3: dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II); barium dihydroxide / acetonitrile; water / 1.75 h / 20 - 80 °C

4: hydrogen; palladium 10% on activated carbon / ethanol; tetrahydrofuran / 63 h / 20 °C

With 2,6-dimethylpyridine; bis-triphenylphosphine-palladium(II) chloride; barium dihydroxide; dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II); palladium 10% on activated carbon; potassium phenolate; hydrogen; triphenylphosphine; In tetrahydrofuran; ethanol; dichloromethane; water; toluene; acetonitrile;

upstream raw materials:

1,3-dimethyl-2,4-dioxo-6-((2-(trimethylsilyl)ethoxy)methyl)-2,3,4,6-tetrahydro-1H-pyrrolo[3,4-d]pyrimidin-5-ylboronic acid

3-(1,3-dimethyl-2,4-dioxo-6-((2-(trimethylsilyl)ethoxy)methyl)-2,3,4,6-tetrahydro-1H-pyrrolo[3,4-d]pyrimidin-5-yl)benzonitrile

3-(1,3-dimethyl-2,4-dioxo-2,3,4,6-tetrahydro-1H-pyrrolo[3,4-d]pyrimidin-5-yl)benzonitrile

methyl 4-(5-(3-cyanophenyl)-1,3-dimethyl-2,4-dioxo-3,4-dihydro-1H-pyrrolo[3,4-d]pyrimidin-6(2H)-yl)butanoate