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

Base Information

Chemical Name:ethyl 5-(1,3-dimethyl-2,4-dioxo-5-phenyl-3,4-dihydro-1H-pyrrolo[3,4-d]pyrimidin-6(2H)-yl)pentanoate
CAS No.:1614252-26-4
Molecular Formula:C₂₁H₂₅N₃O₄
Molecular Weight:383.447
Hs Code.:

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

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

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

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

: 29840-57-1
5-aminovaleric acid ethyl ester hydrochloride

: 443667-38-7
5-benzoyl-6-(bromomethyl)-1,3-dimethylpyrimidine-2,4(1H,3H)-dione

: 1614252-26-4
ethyl 5-(1,3-dimethyl-2,4-dioxo-5-phenyl-3,4-dihydro-1H-pyrrolo[3,4-d]pyrimidin-6(2H)-yl)pentanoate

Guidance literature:: With triethylamine; In ethanol; for 0.666667h; Reflux;

Reference yield:

: 13509-52-9
1,3,6-trimethyluracil

: 1614252-26-4
ethyl 5-(1,3-dimethyl-2,4-dioxo-5-phenyl-3,4-dihydro-1H-pyrrolo[3,4-d]pyrimidin-6(2H)-yl)pentanoate

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 / 0.67 h / Reflux

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

Reference yield:

: 444058-30-4
5-benzoyl-1,3,6-trimethylpyrimidine-2,4(1H,3H)-dione

: 1614252-26-4
ethyl 5-(1,3-dimethyl-2,4-dioxo-5-phenyl-3,4-dihydro-1H-pyrrolo[3,4-d]pyrimidin-6(2H)-yl)pentanoate

Guidance literature:: Multi-step reaction with 2 steps

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

2: triethylamine / ethanol / 0.67 h / Reflux

With bromine; triethylamine; In ethanol; chloroform;