5-(3-chloro-5-fluorophenyl)-4-(3-cyano-4-fluorophenyl)-1,3-thiazole-2-carboxylic acid

Base Information

Chemical Name:5-(3-chloro-5-fluorophenyl)-4-(3-cyano-4-fluorophenyl)-1,3-thiazole-2-carboxylic acid
CAS No.:1266520-44-8
Molecular Formula:C₁₇H₇ClF₂N₂O₂S
Molecular Weight:376.771
Hs Code.:

Synonyms:5-(3-chloro-5-fluorophenyl)-4-(3-cyano-4-fluorophenyl)-1,3-thiazole-2-carboxylic acid

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Chemical Property of 5-(3-chloro-5-fluorophenyl)-4-(3-cyano-4-fluorophenyl)-1,3-thiazole-2-carboxylic acid

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Technology Process of 5-(3-chloro-5-fluorophenyl)-4-(3-cyano-4-fluorophenyl)-1,3-thiazole-2-carboxylic acid

There total 4 articles about 5-(3-chloro-5-fluorophenyl)-4-(3-cyano-4-fluorophenyl)-1,3-thiazole-2-carboxylic acid 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:

: 1266520-43-7
ethyl 5-bromo-4-(3-cyano-4-fluorophenyl)-1,3-thiazole-2-carboxylate

: 328956-61-2
3-fluoro-5-chlorophenylboronic acid

: 1266520-44-8
5-(3-chloro-5-fluorophenyl)-4-(3-cyano-4-fluorophenyl)-1,3-thiazole-2-carboxylic acid

Guidance literature:: With tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium hydrogencarbonate; In 1,2-dimethoxyethane; water; at 20 ℃; for 1h; Reflux;

Reference yield:

: 179897-89-3
5-Bromo-2-fluoro-benzonitrile

: 1266520-44-8
5-(3-chloro-5-fluorophenyl)-4-(3-cyano-4-fluorophenyl)-1,3-thiazole-2-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl / toluene / Inert atmosphere; Reflux

1.2: 4 h / 20 °C

2.1: bromine; hydrogenchloride; acetic acid / water / 1.5 h / 20 °C

2.2: 5 h / Reflux

3.1: bromine; potassium acetate; acetic acid / 48 h / 100 °C

4.1: sodium hydrogencarbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,2-dimethoxyethane; water / 1 h / 20 °C / Reflux

With hydrogenchloride; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; tetrakis(triphenylphosphine) palladium⁽⁰⁾; bromine; potassium acetate; sodium hydrogencarbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; acetic acid; In 1,2-dimethoxyethane; water; toluene;

Reference yield:

: 288309-07-9
3-acetyl-6-fluorobenzenecarbonitrile

: 1266520-44-8
5-(3-chloro-5-fluorophenyl)-4-(3-cyano-4-fluorophenyl)-1,3-thiazole-2-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: bromine; hydrogenchloride; acetic acid / water / 1.5 h / 20 °C

1.2: 5 h / Reflux

2.1: bromine; potassium acetate; acetic acid / 48 h / 100 °C

3.1: sodium hydrogencarbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,2-dimethoxyethane; water / 1 h / 20 °C / Reflux

With hydrogenchloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; bromine; potassium acetate; sodium hydrogencarbonate; acetic acid; In 1,2-dimethoxyethane; water;