ethyl 2-{4-[(1,3-dioxoisoindolin-2-yl)methyl]-2-phenylthiazol-5-yl}acetate

Base Information

Chemical Name:ethyl 2-{4-[(1,3-dioxoisoindolin-2-yl)methyl]-2-phenylthiazol-5-yl}acetate
CAS No.:1447966-52-0
Molecular Formula:C₂₂H₁₈N₂O₄S
Molecular Weight:406.462
Hs Code.:

Synonyms:ethyl 2-{4-[(1,3-dioxoisoindolin-2-yl)methyl]-2-phenylthiazol-5-yl}acetate

Suppliers and Price of ethyl 2-{4-[(1,3-dioxoisoindolin-2-yl)methyl]-2-phenylthiazol-5-yl}acetate

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 ethyl 2-{4-[(1,3-dioxoisoindolin-2-yl)methyl]-2-phenylthiazol-5-yl}acetate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of ethyl 2-{4-[(1,3-dioxoisoindolin-2-yl)methyl]-2-phenylthiazol-5-yl}acetate

There total 5 articles about ethyl 2-{4-[(1,3-dioxoisoindolin-2-yl)methyl]-2-phenylthiazol-5-yl}acetate 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: 76.0%

: 1447966-39-3
ethyl 3-bromo-5-(1,3-dioxoisoindolin-2-yl)-4-oxopentanoate

: 2227-79-4
benzenecarbothioamide

: 1447966-52-0
ethyl 2-{4-[(1,3-dioxoisoindolin-2-yl)methyl]-2-phenylthiazol-5-yl}acetate

Guidance literature:: With 1-butyl-3-methylimidazolium Tetrafluoroborate; at 60 ℃; for 12h;
DOI:10.1016/j.tet.2013.06.060

Reference yield:

: 1074-82-4
potassium phtalimide

: 1447966-52-0
ethyl 2-{4-[(1,3-dioxoisoindolin-2-yl)methyl]-2-phenylthiazol-5-yl}acetate

Guidance literature:: Multi-step reaction with 3 steps

1.1: Br⁺

1.2: 20 °C / Cooling with ice

2.1: 1-butyl-3-methylimidazolium Tetrafluoroborate; hydrogen bromide; bromine / diethyl ether / 0.5 h / Reflux

3.1: 1-butyl-3-methylimidazolium Tetrafluoroborate / 12 h / 60 °C

With hydrogen bromide; bromine; 1-butyl-3-methylimidazolium Tetrafluoroborate; In diethyl ether; 3.1: |Hantzsch Thiazole Synthesis;
DOI:10.1016/j.tet.2013.06.060

Reference yield:

: 65706-98-1
ethyl 5-(1,3-dioxoisoindolin-2-yl)-4-oxopentanoate

: 1447966-52-0
ethyl 2-{4-[(1,3-dioxoisoindolin-2-yl)methyl]-2-phenylthiazol-5-yl}acetate

Guidance literature:: Multi-step reaction with 2 steps

1: 1-butyl-3-methylimidazolium Tetrafluoroborate; hydrogen bromide; bromine / diethyl ether / 0.5 h / Reflux

2: 1-butyl-3-methylimidazolium Tetrafluoroborate / 12 h / 60 °C

With hydrogen bromide; bromine; 1-butyl-3-methylimidazolium Tetrafluoroborate; In diethyl ether; 2: |Hantzsch Thiazole Synthesis;
DOI:10.1016/j.tet.2013.06.060