5-(3-(tert-butylcarbamoyl)-5-(trifluoromethyl)phenyl)-1-(cyclohexylmethyl)-2-methyl-N-(oxetan-3-yl)-1H-pyrrole-3-carboxamide

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Chemical Name:5-(3-(tert-butylcarbamoyl)-5-(trifluoromethyl)phenyl)-1-(cyclohexylmethyl)-2-methyl-N-(oxetan-3-yl)-1H-pyrrole-3-carboxamide
CAS No.:1442425-39-9
Molecular Formula:C₂₈H₃₆F₃N₃O₃
Molecular Weight:519.607
Hs Code.:

Synonyms:5-(3-(tert-butylcarbamoyl)-5-(trifluoromethyl)phenyl)-1-(cyclohexylmethyl)-2-methyl-N-(oxetan-3-yl)-1H-pyrrole-3-carboxamide

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Chemical Property of 5-(3-(tert-butylcarbamoyl)-5-(trifluoromethyl)phenyl)-1-(cyclohexylmethyl)-2-methyl-N-(oxetan-3-yl)-1H-pyrrole-3-carboxamide

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Technology Process of 5-(3-(tert-butylcarbamoyl)-5-(trifluoromethyl)phenyl)-1-(cyclohexylmethyl)-2-methyl-N-(oxetan-3-yl)-1H-pyrrole-3-carboxamide

There total 5 articles about 5-(3-(tert-butylcarbamoyl)-5-(trifluoromethyl)phenyl)-1-(cyclohexylmethyl)-2-methyl-N-(oxetan-3-yl)-1H-pyrrole-3-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: 26.0%

: 1442425-37-7
3-(1-(cyclohexylmethyl)-5-methyl-4-(oxetan-3-ylcarbamoyl)-1H-pyrrol-2-yl)-5-(trifluoromethyl)benzoic acid

: 75-64-9
tert-butylamine

: 1442425-39-9
5-(3-(tert-butylcarbamoyl)-5-(trifluoromethyl)phenyl)-1-(cyclohexylmethyl)-2-methyl-N-(oxetan-3-yl)-1H-pyrrole-3-carboxamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 20 ℃; for 0.333333h;

Reference yield:

: 1442432-65-6
5-bromo-1-(cyclohexylmethyl)-2-methyl-N-(oxetan-3-yl)-1H-pyrrole-3-carboxamide

: 1442425-39-9
5-(3-(tert-butylcarbamoyl)-5-(trifluoromethyl)phenyl)-1-(cyclohexylmethyl)-2-methyl-N-(oxetan-3-yl)-1H-pyrrole-3-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: bis-triphenylphosphine-palladium(II) chloride; tetrabutylammomium bromide; potassium carbonate / 1,4-dioxane; water / 1.5 h / 100 °C / Inert atmosphere; Microwave irradiation

2: lithium hydroxide monohydrate; water / tetrahydrofuran / 3 h / 60 °C

3: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 0.33 h / 20 °C

With bis-triphenylphosphine-palladium(II) chloride; lithium hydroxide monohydrate; tetrabutylammomium bromide; water; potassium carbonate; N-ethyl-N,N-diisopropylamine; HATU; In tetrahydrofuran; 1,4-dioxane; water; N,N-dimethyl-formamide;

Reference yield:

: 1442432-64-5
1-(cyclohexylmethyl)-2-methyl-N-(oxetan-3-yl)-1H-pyrrole-3-carboxamide

: 1442425-39-9
5-(3-(tert-butylcarbamoyl)-5-(trifluoromethyl)phenyl)-1-(cyclohexylmethyl)-2-methyl-N-(oxetan-3-yl)-1H-pyrrole-3-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: N-Bromosuccinimide / tetrahydrofuran / 0.08 h / -78 °C / Inert atmosphere

2: bis-triphenylphosphine-palladium(II) chloride; tetrabutylammomium bromide; potassium carbonate / 1,4-dioxane; water / 1.5 h / 100 °C / Inert atmosphere; Microwave irradiation

3: lithium hydroxide monohydrate; water / tetrahydrofuran / 3 h / 60 °C

4: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 0.33 h / 20 °C

With bis-triphenylphosphine-palladium(II) chloride; N-Bromosuccinimide; lithium hydroxide monohydrate; tetrabutylammomium bromide; water; potassium carbonate; N-ethyl-N,N-diisopropylamine; HATU; In tetrahydrofuran; 1,4-dioxane; water; N,N-dimethyl-formamide;