4-(6-(4-bromophenyl)imidazo[2,1-b]thiazol-5-yl)-N-(4-chlorophenyl)thiazol-2-amine

Base Information

Chemical Name:4-(6-(4-bromophenyl)imidazo[2,1-b]thiazol-5-yl)-N-(4-chlorophenyl)thiazol-2-amine
CAS No.:1395225-89-4
Molecular Formula:C₂₀H₁₂BrClN₄S₂
Molecular Weight:487.831
Hs Code.:

Synonyms:4-(6-(4-bromophenyl)imidazo[2,1-b]thiazol-5-yl)-N-(4-chlorophenyl)thiazol-2-amine

Suppliers and Price of 4-(6-(4-bromophenyl)imidazo[2,1-b]thiazol-5-yl)-N-(4-chlorophenyl)thiazol-2-amine

Supply Marketing:

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

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Total 2 raw suppliers

Chemical Property of 4-(6-(4-bromophenyl)imidazo[2,1-b]thiazol-5-yl)-N-(4-chlorophenyl)thiazol-2-amine

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Hazard Codes:

MSDS Files:

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Technology Process of 4-(6-(4-bromophenyl)imidazo[2,1-b]thiazol-5-yl)-N-(4-chlorophenyl)thiazol-2-amine

There total 3 articles about 4-(6-(4-bromophenyl)imidazo[2,1-b]thiazol-5-yl)-N-(4-chlorophenyl)thiazol-2-amine 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: 89.0%

: 1395225-97-4
1-(6-(4-bromophenyl)imidazo[2,1-b]thiazol-5-yl)-2-chloroethanone

: 3696-23-9
N-(4-chlorophenyl)thiourea

: 1395225-89-4
4-(6-(4-bromophenyl)imidazo[2,1-b]thiazol-5-yl)-N-(4-chlorophenyl)thiazol-2-amine

Guidance literature:: In methanol; at 90 ℃; for 0.5h; under 12929 Torr; Microwave irradiation;
DOI:10.1016/j.tetlet.2012.06.116

Reference yield:

: 99-73-0,132309-76-3
para-bromophenacyl bromide

: 1395225-89-4
4-(6-(4-bromophenyl)imidazo[2,1-b]thiazol-5-yl)-N-(4-chlorophenyl)thiazol-2-amine

Guidance literature:: Multi-step reaction with 3 steps

1.1: acetone / Reflux

1.2: Reflux

2.1: 1,4-dioxane / 5.5 h / 70 - 104 °C

3.1: methanol / 0.5 h / 90 °C / 12929 Torr / Microwave irradiation

In 1,4-dioxane; methanol; acetone; 3.1: |Hantzsch Thiazole Synthesis;
DOI:10.1016/j.tetlet.2012.06.116

Reference yield:

: 7120-13-0
6-(4-bromophenyl)imidazo[2,1-b][1,3]thiazole

: 1395225-89-4
4-(6-(4-bromophenyl)imidazo[2,1-b]thiazol-5-yl)-N-(4-chlorophenyl)thiazol-2-amine

Guidance literature:: Multi-step reaction with 2 steps

1: 1,4-dioxane / 5.5 h / 70 - 104 °C

2: methanol / 0.5 h / 90 °C / 12929 Torr / Microwave irradiation

In 1,4-dioxane; methanol; 2: |Hantzsch Thiazole Synthesis;
DOI:10.1016/j.tetlet.2012.06.116