N-((2-(benzo[d][1,3]dioxol-5-yl)-6-phenylimidazo[2,1-b][1,3,4]thiadiazol-5-yl)methylene)-4-bromoaniline

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Chemical Name:N-((2-(benzo[d][1,3]dioxol-5-yl)-6-phenylimidazo[2,1-b][1,3,4]thiadiazol-5-yl)methylene)-4-bromoaniline
CAS No.:1448158-14-2
Molecular Formula:C₂₄H₁₅BrN₄O₂S
Molecular Weight:503.379
Hs Code.:

Synonyms:N-((2-(benzo[d][1,3]dioxol-5-yl)-6-phenylimidazo[2,1-b][1,3,4]thiadiazol-5-yl)methylene)-4-bromoaniline

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Chemical Property of N-((2-(benzo[d][1,3]dioxol-5-yl)-6-phenylimidazo[2,1-b][1,3,4]thiadiazol-5-yl)methylene)-4-bromoaniline

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Technology Process of N-((2-(benzo[d][1,3]dioxol-5-yl)-6-phenylimidazo[2,1-b][1,3,4]thiadiazol-5-yl)methylene)-4-bromoaniline

There total 2 articles about N-((2-(benzo[d][1,3]dioxol-5-yl)-6-phenylimidazo[2,1-b][1,3,4]thiadiazol-5-yl)methylene)-4-bromoaniline 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: 78.0%

: 2-(benzo[d][1,3]dioxol-5-yl)-6-phenylimidazo[2,1-b][1,3,4]thiadiazole-5-carbaldehyde

: 106-40-1
4-bromo-aniline

: 1448158-14-2
N-((2-(benzo[d][1,3]dioxol-5-yl)-6-phenylimidazo[2,1-b][1,3,4]thiadiazol-5-yl)methylene)-4-bromoaniline

Guidance literature:: With acetic acid; In ethanol; for 6h; Reflux;
DOI:10.1016/j.ejmech.2013.04.020

Reference yield:

: 83796-52-5
2-(3,4-dioxymethylenephenyl)-6-phenylimidazo<2,1-b>-1,3,4-thiadiazole

: 1448158-14-2
N-((2-(benzo[d][1,3]dioxol-5-yl)-6-phenylimidazo[2,1-b][1,3,4]thiadiazol-5-yl)methylene)-4-bromoaniline

Guidance literature:: Multi-step reaction with 2 steps

1: trichlorophosphate

2: acetic acid / ethanol / 6 h / Reflux

With acetic acid; trichlorophosphate; In ethanol; 1: |Vilsmeier-Haack Formylation;
DOI:10.1016/j.ejmech.2013.04.020