N-[3-(1H-6-nitroindazol-1-yl)-propyl]-2-(3-bromophenyl)-4-oxo-5-(3-bromobenzylidene)-1,3-thiazolidine-carboxamide

Base Information

Chemical Name:N-[3-(1H-6-nitroindazol-1-yl)-propyl]-2-(3-bromophenyl)-4-oxo-5-(3-bromobenzylidene)-1,3-thiazolidine-carboxamide
CAS No.:1380421-86-2
Molecular Formula:C₂₇H₂₁Br₂N₅O₄S
Molecular Weight:671.369
Hs Code.:

Synonyms:N-[3-(1H-6-nitroindazol-1-yl)-propyl]-2-(3-bromophenyl)-4-oxo-5-(3-bromobenzylidene)-1,3-thiazolidine-carboxamide

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Chemical Property of N-[3-(1H-6-nitroindazol-1-yl)-propyl]-2-(3-bromophenyl)-4-oxo-5-(3-bromobenzylidene)-1,3-thiazolidine-carboxamide

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Technology Process of N-[3-(1H-6-nitroindazol-1-yl)-propyl]-2-(3-bromophenyl)-4-oxo-5-(3-bromobenzylidene)-1,3-thiazolidine-carboxamide

There total 5 articles about N-[3-(1H-6-nitroindazol-1-yl)-propyl]-2-(3-bromophenyl)-4-oxo-5-(3-bromobenzylidene)-1,3-thiazolidine-carboxamide 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: 61.0%

: 3132-99-8
m-bromobenzoic aldehyde

: 1380421-76-0
N-[3-(1H-6-nitroindazol-1-yl)-propyl]-2-(3-bromophenyl)-4-oxo-1,3-thiazolidine-carboxamide

: 1380421-86-2
N-[3-(1H-6-nitroindazol-1-yl)-propyl]-2-(3-bromophenyl)-4-oxo-5-(3-bromobenzylidene)-1,3-thiazolidine-carboxamide

Guidance literature:: With sodium ethanolate; In ethanol; at 20 ℃; for 6.3h; Reflux;
DOI:10.4067/s0717-97072012000100018

Reference yield:

: 1016495-42-3
N₁-(3-chloropropyl)-6-nitroindazole

: 1380421-86-2
N-[3-(1H-6-nitroindazol-1-yl)-propyl]-2-(3-bromophenyl)-4-oxo-5-(3-bromobenzylidene)-1,3-thiazolidine-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: ethanol / 4.3 h / 20 °C

2: acetic acid / ethanol / 4.3 h / Reflux

3: zinc(II) chloride / ethanol / 7.3 h / 20 °C / Reflux

4: sodium ethanolate / ethanol / 6.3 h / 20 °C / Reflux

With sodium ethanolate; acetic acid; zinc(II) chloride; In ethanol; 4: Knoevenagel condensation;
DOI:10.4067/s0717-97072012000100018

Reference yield:

: 1360889-31-1
N-[3-(1H-6-nitroindazol-1-yl)-propyl]-N'-[(3-bromophenyl)-methylidene]-urea

: 1380421-86-2
N-[3-(1H-6-nitroindazol-1-yl)-propyl]-2-(3-bromophenyl)-4-oxo-5-(3-bromobenzylidene)-1,3-thiazolidine-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: zinc(II) chloride / ethanol / 7.3 h / 20 °C / Reflux

2: sodium ethanolate / ethanol / 6.3 h / 20 °C / Reflux

With sodium ethanolate; zinc(II) chloride; In ethanol; 2: Knoevenagel condensation;
DOI:10.4067/s0717-97072012000100018