3-benzyl-6-bromo-2-(1-bromopropyl)-5-methylpyrrolo[2,3-e]pyrimidin-4-one

Base Information

Chemical Name:3-benzyl-6-bromo-2-(1-bromopropyl)-5-methylpyrrolo[2,3-e]pyrimidin-4-one
CAS No.:1333405-31-4
Molecular Formula:C₁₇H₁₇Br₂N₃O
Molecular Weight:439.149
Hs Code.:

Synonyms:3-benzyl-6-bromo-2-(1-bromopropyl)-5-methylpyrrolo[2,3-e]pyrimidin-4-one

Suppliers and Price of 3-benzyl-6-bromo-2-(1-bromopropyl)-5-methylpyrrolo[2,3-e]pyrimidin-4-one

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 3-benzyl-6-bromo-2-(1-bromopropyl)-5-methylpyrrolo[2,3-e]pyrimidin-4-one

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 3-benzyl-6-bromo-2-(1-bromopropyl)-5-methylpyrrolo[2,3-e]pyrimidin-4-one

There total 5 articles about 3-benzyl-6-bromo-2-(1-bromopropyl)-5-methylpyrrolo[2,3-e]pyrimidin-4-one 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: 95.0%

: 1333405-30-3
3-benzyl-6-bromo-5-methyl-2-propylpyrrolo[2,3-e]pyrimidin-4-one

: 1333405-31-4
3-benzyl-6-bromo-2-(1-bromopropyl)-5-methylpyrrolo[2,3-e]pyrimidin-4-one

Guidance literature:: With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; for 0.75h; Reflux;
DOI:10.1021/jm200629m

Reference yield:

: 1333405-25-6
ethyl 3-(butanoylamino)-1H-pyrrole-2-carboxylate

: 1333405-31-4
3-benzyl-6-bromo-2-(1-bromopropyl)-5-methylpyrrolo[2,3-e]pyrimidin-4-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: benzyl tri-n-butylammonium bromide; sodium hydroxide / dichloromethane / 3 h / 0 - 25 °C

2.1: ammonium hydroxide / 6 h / 110 - 115 °C

3.1: tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate / toluene / 16 h / Reflux

3.2: 0.08 h / 65 °C

4.1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 0.75 h / Reflux

With ammonium hydroxide; N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); tetra(n-butyl)ammonium hydrogensulfate; benzyl tri-n-butylammonium bromide; potassium carbonate; sodium hydroxide; In tetrachloromethane; dichloromethane; toluene;
DOI:10.1021/jm200629m

Reference yield:

: 1333405-27-8
5-methyl-2-propyl-3H-pyrrolo[2,3-e]pyrimidin-4-one

: 1333405-31-4
3-benzyl-6-bromo-2-(1-bromopropyl)-5-methylpyrrolo[2,3-e]pyrimidin-4-one

Guidance literature:: Multi-step reaction with 2 steps

1.1: tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate / toluene / 16 h / Reflux

1.2: 0.08 h / 65 °C

2.1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 0.75 h / Reflux

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate; In tetrachloromethane; toluene;
DOI:10.1021/jm200629m