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

Base Information

• Chemical Name: methyl 3-(1,3-dimethyl-2,4-dioxo-5-phenyl-3,4-dihydro-1H-pyrrolo[3,4-d]pyrimidin-6(2H)-yl)propanoate
• CAS No.: 1614251-54-5
• Molecular Formula: C₁₈H₁₉N₃O₄
• Molecular Weight: 341.367
• Mol file: 1614251-54-5.mol

Synonyms:methyl 3-(1,3-dimethyl-2,4-dioxo-5-phenyl-3,4-dihydro-1H-pyrrolo[3,4-d]pyrimidin-6(2H)-yl)propanoate

Chemical Property of methyl 3-(1,3-dimethyl-2,4-dioxo-5-phenyl-3,4-dihydro-1H-pyrrolo[3,4-d]pyrimidin-6(2H)-yl)propanoate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of methyl 3-(1,3-dimethyl-2,4-dioxo-5-phenyl-3,4-dihydro-1H-pyrrolo[3,4-d]pyrimidin-6(2H)-yl)propanoate

There total 3 articles about methyl 3-(1,3-dimethyl-2,4-dioxo-5-phenyl-3,4-dihydro-1H-pyrrolo[3,4-d]pyrimidin-6(2H)-yl)propanoate 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:

methyl 3-aminopropanoate hydrochloride (3196-73-4) + 5-benzoyl-6-(bromomethyl)-1,3-dimethylpyrimidine-2,4(1H,3H)-dione (443667-38-7) → methyl 3-(1,3-dimethyl-2,4-dioxo-5-phenyl-3,4-dihydro-1H-pyrrolo[3,4-d]pyrimidin-6(2H)-yl)propanoate (1614251-54-5)

Guidance literature:

With triethylamine; In ethanol; at 100 ℃; for 1.5h; Microwave irradiation;

Reference yield:

1,3,6-trimethyluracil (13509-52-9) → methyl 3-(1,3-dimethyl-2,4-dioxo-5-phenyl-3,4-dihydro-1H-pyrrolo[3,4-d]pyrimidin-6(2H)-yl)propanoate (1614251-54-5)

Guidance literature:

Multi-step reaction with 3 steps

1: zinc(II) chloride / chlorobenzene / 16 h / 110 °C / Inert atmosphere

2: bromine / chloroform / 2.5 h / 55 °C / Inert atmosphere

3: triethylamine / ethanol / 1.5 h / 100 °C / Microwave irradiation

With bromine; triethylamine; zinc(II) chloride; In ethanol; chloroform; chlorobenzene;

Reference yield:

5-benzoyl-1,3,6-trimethylpyrimidine-2,4(1H,3H)-dione (444058-30-4) → methyl 3-(1,3-dimethyl-2,4-dioxo-5-phenyl-3,4-dihydro-1H-pyrrolo[3,4-d]pyrimidin-6(2H)-yl)propanoate (1614251-54-5)

Guidance literature:

Multi-step reaction with 2 steps

1: bromine / chloroform / 2.5 h / 55 °C / Inert atmosphere

2: triethylamine / ethanol / 1.5 h / 100 °C / Microwave irradiation

With bromine; triethylamine; In ethanol; chloroform;

upstream raw materials:

1,3,6-trimethyluracil

5-benzoyl-1,3,6-trimethylpyrimidine-2,4(1H,3H)-dione

methyl 3-aminopropanoate hydrochloride

5-benzoyl-6-(bromomethyl)-1,3-dimethylpyrimidine-2,4(1H,3H)-dione

Downstream raw materials:

3-(1,3-dimethyl-2,4-dioxo-5-phenyl-3,4-dihydro-1H-pyrrolo[3,4-d]pyrimidin-6(2H)-yl)-N-methoxy-N-methylpropanamide

9-(4-chlorothiazol-2-yl)-1,3-dimethyl-5-phenyl-8,9-dihydro-1H-pyrimido[4,5-a]pyrrolizine-2,4(3H,7H)-dione

6-(3-(4-chlorothiazol-2-yl)-3-hydroxypropyl)-1,3-dimethyl-5-phenyl-1H-pyrrolo[3,4-d]pyrimidine-2,4(3H,6H)-dione

6-(3-(4-chlorothiazol-2-yl)-3-oxopropyl)-1,3-dimethyl-5-phenyl-1H-pyrrolo[3,4-d]pyrimidine-2,4(3H,6H)-dione