(S)-N-(1-(3-(3-chloro-4-cyanophenyl)-1H-pyrazol-1-yl)propan-2-yl)-2-((2,5-dioxopyrrolidin-1-yl)methyl)oxazole-4-carboxamide

Base Information

Chemical Name:(S)-N-(1-(3-(3-chloro-4-cyanophenyl)-1H-pyrazol-1-yl)propan-2-yl)-2-((2,5-dioxopyrrolidin-1-yl)methyl)oxazole-4-carboxamide
CAS No.:1297542-94-9
Molecular Formula:C₂₂H₁₉ClN₆O₄
Molecular Weight:466.884
Hs Code.:

Synonyms:(S)-N-(1-(3-(3-chloro-4-cyanophenyl)-1H-pyrazol-1-yl)propan-2-yl)-2-((2,5-dioxopyrrolidin-1-yl)methyl)oxazole-4-carboxamide

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Chemical Property of (S)-N-(1-(3-(3-chloro-4-cyanophenyl)-1H-pyrazol-1-yl)propan-2-yl)-2-((2,5-dioxopyrrolidin-1-yl)methyl)oxazole-4-carboxamide

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Technology Process of (S)-N-(1-(3-(3-chloro-4-cyanophenyl)-1H-pyrazol-1-yl)propan-2-yl)-2-((2,5-dioxopyrrolidin-1-yl)methyl)oxazole-4-carboxamide

There total 8 articles about (S)-N-(1-(3-(3-chloro-4-cyanophenyl)-1H-pyrazol-1-yl)propan-2-yl)-2-((2,5-dioxopyrrolidin-1-yl)methyl)oxazole-4-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: 16.92%

: 123-56-8,89963-74-6
Succinimide

: 1297542-22-3
(S)-N-(1-(3-(3-chloro-4-cyanophenyl)-1H-pyrazol-1-yl)propan-2-yl)-2-(chloromethyl)oxazole-4-carboxamide

: 1297542-94-9
(S)-N-(1-(3-(3-chloro-4-cyanophenyl)-1H-pyrazol-1-yl)propan-2-yl)-2-((2,5-dioxopyrrolidin-1-yl)methyl)oxazole-4-carboxamide

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 4.5h; Inert atmosphere;

Reference yield:

: 154607-01-9
4-bromo-2-chlorobenzonitrile

: 1297542-94-9
(S)-N-(1-(3-(3-chloro-4-cyanophenyl)-1H-pyrazol-1-yl)propan-2-yl)-2-((2,5-dioxopyrrolidin-1-yl)methyl)oxazole-4-carboxamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium carbonate / bis-triphenylphosphine-palladium(II) chloride / water; tetrahydrofuran / 2.5 h / 35 °C

2.1: hydrogenchloride / ethanol / 1 h / 30 °C / Inert atmosphere

3.1: sodium hydroxide / water; methanol / 2 h / 25 °C / Inert atmosphere

4.1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 18 h / 20 °C / Inert atmosphere

4.2: 20 h / 20 °C

5.1: dicyclohexyl-carbodiimide / dichloromethane / 20 °C

6.1: potassium carbonate / N,N-dimethyl-formamide / 4.5 h / 20 °C / Inert atmosphere

With hydrogenchloride; di-isopropyl azodicarboxylate; sodium carbonate; potassium carbonate; dicyclohexyl-carbodiimide; triphenylphosphine; sodium hydroxide; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

: 208465-72-9
methyl 2-(chloromethyl)-1,3-oxazole-4-carboxylate

: 1297542-94-9
(S)-N-(1-(3-(3-chloro-4-cyanophenyl)-1H-pyrazol-1-yl)propan-2-yl)-2-((2,5-dioxopyrrolidin-1-yl)methyl)oxazole-4-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: lithium hydroxide / tetrahydrofuran; methanol / 1 h / 20 °C

1.2: pH 1.5 / Acidic conditions

2.1: dicyclohexyl-carbodiimide / dichloromethane / 20 °C

3.1: potassium carbonate / N,N-dimethyl-formamide / 4.5 h / 20 °C / Inert atmosphere

With potassium carbonate; dicyclohexyl-carbodiimide; lithium hydroxide; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;