1H-indole-3-carbaldehyde [4-(4-chlorophenyl)-1,3-thiazol-2-yl]hydrazone

Base Information

Chemical Name:1H-indole-3-carbaldehyde [4-(4-chlorophenyl)-1,3-thiazol-2-yl]hydrazone
CAS No.:307544-76-9
Molecular Formula:C₁₈H₁₃ClN₄S
Molecular Weight:352.847
Hs Code.:
Mol file:307544-76-9.mol

Synonyms:1-((1H-indol-3-yl)methylene)-2-(4-(4-chlorophenyl)thiazol-2-yl)hydrazine

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Chemical Property of 1H-indole-3-carbaldehyde [4-(4-chlorophenyl)-1,3-thiazol-2-yl]hydrazone

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Technology Process of 1H-indole-3-carbaldehyde [4-(4-chlorophenyl)-1,3-thiazol-2-yl]hydrazone

There total 3 articles about 1H-indole-3-carbaldehyde [4-(4-chlorophenyl)-1,3-thiazol-2-yl]hydrazone 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: 98.0%

: 937-20-2
p-chlorophenacyl chloride

: 6868-28-6
2-((1H-indol-3-yl)methylene)hydrazine-1-carbothioamide

: 307544-76-9
1-((1H-indol-3-yl)methylene)-2-(4-(4-chlorophenyl)thiazol-2-yl)hydrazine

Guidance literature:: In ethanol; at 20 ℃;
DOI:10.1016/j.bmc.2014.01.022

Reference yield:

: 536-38-9
4-chlorobenzoylmethyl bromide

: 6868-28-6
2-((1H-indol-3-yl)methylene)hydrazine-1-carbothioamide

: 307544-76-9
1-((1H-indol-3-yl)methylene)-2-(4-(4-chlorophenyl)thiazol-2-yl)hydrazine

Guidance literature:: 4-chlorobenzoylmethyl bromide; 2-((1H-indol-3-yl)methylene)hydrazine-1-carbothioamide; In methanol; for 0.0166667h;

In methanol; at 90 ℃; for 0.166667h; Microwave irradiation;
DOI:10.1016/j.ejmech.2014.04.042

Reference yield:

: 487-89-8,1228547-52-1
Indole-3-carboxaldehyde

: 307544-76-9
1-((1H-indol-3-yl)methylene)-2-(4-(4-chlorophenyl)thiazol-2-yl)hydrazine

Guidance literature:: Multi-step reaction with 2 steps

1: acetic acid / ethanol / 20 °C

2: ethanol / 20 °C

With acetic acid; In ethanol;
DOI:10.1016/j.bmc.2014.01.022