(2-chlorophenyl)-N-{5-[1-methyl-3-(5-methyl(1,2,4,-oxadiazol-3-yl))pyrazol-5-yl](1,3-thiazol-2-yl)}carboxamide

Base Information

Chemical Name:(2-chlorophenyl)-N-{5-[1-methyl-3-(5-methyl(1,2,4,-oxadiazol-3-yl))pyrazol-5-yl](1,3-thiazol-2-yl)}carboxamide
CAS No.:1361379-23-8
Molecular Formula:C₁₇H₁₃ClN₆O₂S
Molecular Weight:400.848
Hs Code.:

Synonyms:(2-chlorophenyl)-N-{5-[1-methyl-3-(5-methyl(1,2,4,-oxadiazol-3-yl))pyrazol-5-yl](1,3-thiazol-2-yl)}carboxamide

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Chemical Property of (2-chlorophenyl)-N-{5-[1-methyl-3-(5-methyl(1,2,4,-oxadiazol-3-yl))pyrazol-5-yl](1,3-thiazol-2-yl)}carboxamide

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Technology Process of (2-chlorophenyl)-N-{5-[1-methyl-3-(5-methyl(1,2,4,-oxadiazol-3-yl))pyrazol-5-yl](1,3-thiazol-2-yl)}carboxamide

There total 4 articles about (2-chlorophenyl)-N-{5-[1-methyl-3-(5-methyl(1,2,4,-oxadiazol-3-yl))pyrazol-5-yl](1,3-thiazol-2-yl)}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: 14.5%

: 1345118-58-2
[1-methyl-3-(5-methyl-1,2,4-oxadiazol-3-yl)]pyrazol-5-yl-boronic acid

: 1184579-73-4
N-(5-bromo(1,3-thiazol-2-yl))(2-chlorophenyl)carboxamide

: 1361379-23-8
(2-chlorophenyl)-N-{5-[1-methyl-3-(5-methyl(1,2,4,-oxadiazol-3-yl))pyrazol-5-yl](1,3-thiazol-2-yl)}carboxamide

Guidance literature:: With potassium phosphate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In water; N,N-dimethyl-formamide; at 150 ℃; for 0.5h; Inert atmosphere; Microwave irradiation;

Reference yield:

: 1345118-56-0
5-methyl-3-(1-methylpyrazol-3-yl)-1,2,4-oxadiazole

: 1361379-23-8
(2-chlorophenyl)-N-{5-[1-methyl-3-(5-methyl(1,2,4,-oxadiazol-3-yl))pyrazol-5-yl](1,3-thiazol-2-yl)}carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: n-butyllithium / hexane; tetrahydrofuran / 3 h / -70 °C

1.2: 20 °C

1.3: pH 2

2.1: potassium phosphate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / N,N-dimethyl-formamide; water / 0.5 h / 150 °C / Inert atmosphere; Microwave irradiation

With potassium phosphate; n-butyllithium; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In tetrahydrofuran; hexane; water; N,N-dimethyl-formamide;

Reference yield:

: 79080-39-0
1-Methylpyrazole-3-carboxylic acid nitrile

: 1361379-23-8
(2-chlorophenyl)-N-{5-[1-methyl-3-(5-methyl(1,2,4,-oxadiazol-3-yl))pyrazol-5-yl](1,3-thiazol-2-yl)}carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydroxylamine hydrochloride; sodium ethanolate / ethanol / 90 °C

2.1: ytterbium(III) triflate / ethanol / 2 h / 85 °C

3.1: n-butyllithium / hexane; tetrahydrofuran / 3 h / -70 °C

3.2: 20 °C

3.3: pH 2

4.1: potassium phosphate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / N,N-dimethyl-formamide; water / 0.5 h / 150 °C / Inert atmosphere; Microwave irradiation

With potassium phosphate; n-butyllithium; hydroxylamine hydrochloride; sodium ethanolate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; ytterbium(III) triflate; In tetrahydrofuran; ethanol; hexane; water; N,N-dimethyl-formamide;