(5Z)-5-({1-[4-Chloro-2-(trifluoromethyl)benzyl]-1H-indazol-5-yl}methylidene)-3-[2-(ethylamino)ethyl]-1,3-thiazolidine-2,4-dione

Base Information

Chemical Name:(5Z)-5-({1-[4-Chloro-2-(trifluoromethyl)benzyl]-1H-indazol-5-yl}methylidene)-3-[2-(ethylamino)ethyl]-1,3-thiazolidine-2,4-dione
CAS No.:1351565-81-5
Molecular Formula:C₂₃H₂₀ClF₃N₄O₂S
Molecular Weight:508.952
Hs Code.:

Synonyms:(5Z)-5-({1-[4-Chloro-2-(trifluoromethyl)benzyl]-1H-indazol-5-yl}methylidene)-3-[2-(ethylamino)ethyl]-1,3-thiazolidine-2,4-dione

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Chemical Property of (5Z)-5-({1-[4-Chloro-2-(trifluoromethyl)benzyl]-1H-indazol-5-yl}methylidene)-3-[2-(ethylamino)ethyl]-1,3-thiazolidine-2,4-dione

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Technology Process of (5Z)-5-({1-[4-Chloro-2-(trifluoromethyl)benzyl]-1H-indazol-5-yl}methylidene)-3-[2-(ethylamino)ethyl]-1,3-thiazolidine-2,4-dione

There total 4 articles about (5Z)-5-({1-[4-Chloro-2-(trifluoromethyl)benzyl]-1H-indazol-5-yl}methylidene)-3-[2-(ethylamino)ethyl]-1,3-thiazolidine-2,4-dione 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:

: 1351564-76-5
(5Z)-5-({1-[4-chloro-2-(trifluoromethyl)benzyl]-1H-indazol-5-yl}methylidene)-2,4-dioxo-1,3-thiazolidine

: 110-73-6
2-(Ethylamino)ethanol

: 1351565-81-5
(5Z)-5-({1-[4-Chloro-2-(trifluoromethyl)benzyl]-1H-indazol-5-yl}methylidene)-3-[2-(ethylamino)ethyl]-1,3-thiazolidine-2,4-dione

Guidance literature:: With di-isopropyl azodicarboxylate; In tetrahydrofuran; at 60 ℃;

Reference yield:

: 253801-04-6
1H-indazole-5-carbaldehyde

: 1351565-81-5
(5Z)-5-({1-[4-Chloro-2-(trifluoromethyl)benzyl]-1H-indazol-5-yl}methylidene)-3-[2-(ethylamino)ethyl]-1,3-thiazolidine-2,4-dione

Guidance literature:: Multi-step reaction with 3 steps

1: caesium carbonate / N,N-dimethyl-formamide / 16 h / 90 °C

2: ammonium acetate; acetic acid / 12 h / 110 °C

3: di-isopropyl azodicarboxylate / tetrahydrofuran / 60 °C

With di-isopropyl azodicarboxylate; ammonium acetate; caesium carbonate; acetic acid; In tetrahydrofuran; N,N-dimethyl-formamide; 3: Mitsunobu reaction;

Reference yield:

: 1312704-84-9
1-[4-chloro-2-(trifluoromethyl)benzyl]-1H-indazole-5-carbaldehyde

: 1351565-81-5
(5Z)-5-({1-[4-Chloro-2-(trifluoromethyl)benzyl]-1H-indazol-5-yl}methylidene)-3-[2-(ethylamino)ethyl]-1,3-thiazolidine-2,4-dione

Guidance literature:: Multi-step reaction with 2 steps

1: ammonium acetate; acetic acid / 12 h / 110 °C

2: di-isopropyl azodicarboxylate / tetrahydrofuran / 60 °C

With di-isopropyl azodicarboxylate; ammonium acetate; acetic acid; In tetrahydrofuran; 2: Mitsunobu reaction;