(5-ethyloxycarbonylimidazo[2,1-b][1,3]thiazol-6-ylmethyl)(triphenyl)phosphonium bromide

Base Information

Chemical Name:(5-ethyloxycarbonylimidazo[2,1-b][1,3]thiazol-6-ylmethyl)(triphenyl)phosphonium bromide
CAS No.:1228828-37-2
Molecular Formula:Br*C₂₇H₂₄N₂O₂PS
Molecular Weight:551.444
Hs Code.:

Synonyms:(5-ethyloxycarbonylimidazo[2,1-b][1,3]thiazol-6-ylmethyl)(triphenyl)phosphonium bromide

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Chemical Property of (5-ethyloxycarbonylimidazo[2,1-b][1,3]thiazol-6-ylmethyl)(triphenyl)phosphonium bromide

Chemical Property:

Purity/Quality:

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Technology Process of (5-ethyloxycarbonylimidazo[2,1-b][1,3]thiazol-6-ylmethyl)(triphenyl)phosphonium bromide

There total 3 articles about (5-ethyloxycarbonylimidazo[2,1-b][1,3]thiazol-6-ylmethyl)(triphenyl)phosphonium bromide 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:

: 1228828-36-1
ethyl 6-bromomethyl imidazo[2,1-b][1,3]thiazole-5-carboxylate

: 603-35-0
triphenylphosphine

: 1228828-37-2
(5-ethyloxycarbonylimidazo[2,1-b][1,3]thiazol-6-ylmethyl)(triphenyl)phosphonium bromide

Guidance literature:: In acetonitrile; at 22 ℃; Reflux;

Reference yield:

: 609-15-4
ethyl 2-chloro-3-oxo-butyrate

: 1228828-37-2
(5-ethyloxycarbonylimidazo[2,1-b][1,3]thiazol-6-ylmethyl)(triphenyl)phosphonium bromide

Guidance literature:: Multi-step reaction with 3 steps

1: ethanol / 24 h / Reflux

2: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 18 h / Reflux

3: acetonitrile / 20 °C / Reflux

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; ethanol; acetonitrile;

Reference yield:

: 57626-37-6
ethyl 6-methylimidazo<2.1-b>thiazole-5-carboxylate

: 1228828-37-2
(5-ethyloxycarbonylimidazo[2,1-b][1,3]thiazol-6-ylmethyl)(triphenyl)phosphonium bromide

Guidance literature:: Multi-step reaction with 2 steps

1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 18 h / Reflux

2: acetonitrile / 20 °C / Reflux

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; acetonitrile;