methyl 6-[[3-(4-acetonyloxyphenyl)-2,5-dioxo-imidazolidin-1-yl]methyl]-7-methyl-pyrrolo[2,3-d]pyrimidine-2-carboxylate

Base Information

Chemical Name:methyl 6-[[3-(4-acetonyloxyphenyl)-2,5-dioxo-imidazolidin-1-yl]methyl]-7-methyl-pyrrolo[2,3-d]pyrimidine-2-carboxylate
CAS No.:1596360-51-8
Molecular Formula:C₂₂H₂₁N₅O₆
Molecular Weight:451.439
Hs Code.:

Synonyms:methyl 6-[[3-(4-acetonyloxyphenyl)-2,5-dioxo-imidazolidin-1-yl]methyl]-7-methyl-pyrrolo[2,3-d]pyrimidine-2-carboxylate

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Chemical Property of methyl 6-[[3-(4-acetonyloxyphenyl)-2,5-dioxo-imidazolidin-1-yl]methyl]-7-methyl-pyrrolo[2,3-d]pyrimidine-2-carboxylate

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Technology Process of methyl 6-[[3-(4-acetonyloxyphenyl)-2,5-dioxo-imidazolidin-1-yl]methyl]-7-methyl-pyrrolo[2,3-d]pyrimidine-2-carboxylate

There total 9 articles about methyl 6-[[3-(4-acetonyloxyphenyl)-2,5-dioxo-imidazolidin-1-yl]methyl]-7-methyl-pyrrolo[2,3-d]pyrimidine-2-carboxylate 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: 69.0%

: 1596360-16-5
methyl 6-(bromomethyl)-7-methyl-7H-pyrrolo[2,3-d]pyrimidine-2-carboxylate

: 1596359-97-5
1-(4-acetonyloxyphenyl)imidazolidine-2,4-dione

: 1596360-51-8
methyl 6-[[3-(4-acetonyloxyphenyl)-2,5-dioxo-imidazolidin-1-yl]methyl]-7-methyl-pyrrolo[2,3-d]pyrimidine-2-carboxylate

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 15h;
DOI:10.1016/j.bmc.2014.02.002

Reference yield:

: 1596360-12-1
5-bromo-4-methylamino-pyrimidine-2-carbonitrile

: 1596360-51-8
methyl 6-[[3-(4-acetonyloxyphenyl)-2,5-dioxo-imidazolidin-1-yl]methyl]-7-methyl-pyrrolo[2,3-d]pyrimidine-2-carboxylate

Guidance literature:: Multi-step reaction with 6 steps

1: hydrogenchloride / 15 h / 20 °C

2: triethylamine; copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide / 4 h / 80 °C

3: 1,8-diazabicyclo[5.4.0]undec-7-ene / N,N-dimethyl-formamide / 2 h / 20 - 100 °C

4: hydrogenchloride; sodium hydrogencarbonate / methanol / 3 h / 20 °C

5: carbon tetrabromide; triphenylphosphine / dichloromethane / 3.5 h / 0 - 20 °C

6: potassium carbonate / N,N-dimethyl-formamide / 15 h / 20 °C

With hydrogenchloride; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; carbon tetrabromide; sodium hydrogencarbonate; potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; triphenylphosphine; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2014.02.002

Reference yield:

: 1596360-88-1
ethyl 2-[(4-acetonyloxyphenyl)amino]acetate

: 1596360-51-8
methyl 6-[[3-(4-acetonyloxyphenyl)-2,5-dioxo-imidazolidin-1-yl]methyl]-7-methyl-pyrrolo[2,3-d]pyrimidine-2-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: acetic acid / 18 h / 20 - 100 °C / Inert atmosphere

2: potassium carbonate / N,N-dimethyl-formamide / 15 h / 20 °C

With potassium carbonate; In acetic acid; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2014.02.002