methyl 3-(1-(cyclohexylmethyl)-5-methyl-4-(oxetan-3-ylcarbamoyl)-1H-pyrrol-2-yl)-5-(trifluoromethyl)benzoate

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Chemical Name:methyl 3-(1-(cyclohexylmethyl)-5-methyl-4-(oxetan-3-ylcarbamoyl)-1H-pyrrol-2-yl)-5-(trifluoromethyl)benzoate
CAS No.:1442425-35-5
Molecular Formula:C₂₅H₂₉F₃N₂O₄
Molecular Weight:478.511
Hs Code.:

Synonyms:methyl 3-(1-(cyclohexylmethyl)-5-methyl-4-(oxetan-3-ylcarbamoyl)-1H-pyrrol-2-yl)-5-(trifluoromethyl)benzoate

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Chemical Property of methyl 3-(1-(cyclohexylmethyl)-5-methyl-4-(oxetan-3-ylcarbamoyl)-1H-pyrrol-2-yl)-5-(trifluoromethyl)benzoate

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Technology Process of methyl 3-(1-(cyclohexylmethyl)-5-methyl-4-(oxetan-3-ylcarbamoyl)-1H-pyrrol-2-yl)-5-(trifluoromethyl)benzoate

There total 3 articles about methyl 3-(1-(cyclohexylmethyl)-5-methyl-4-(oxetan-3-ylcarbamoyl)-1H-pyrrol-2-yl)-5-(trifluoromethyl)benzoate 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: 63.0%

: 1150271-61-6
methyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5-(trifluoromethyl)benzoate

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

: 1442425-35-5
methyl 3-(1-(cyclohexylmethyl)-5-methyl-4-(oxetan-3-ylcarbamoyl)-1H-pyrrol-2-yl)-5-(trifluoromethyl)benzoate

Guidance literature:: With bis-triphenylphosphine-palladium(II) chloride; tetrabutylammomium bromide; potassium carbonate; In 1,4-dioxane; water; at 100 ℃; for 1.5h; Inert atmosphere; Microwave irradiation;

Reference yield:

: 1442432-63-4
1-(cyclohexylmethyl)-2-methyl-1H-pyrrole-3-carboxylic acid

: 1442425-35-5
methyl 3-(1-(cyclohexylmethyl)-5-methyl-4-(oxetan-3-ylcarbamoyl)-1H-pyrrol-2-yl)-5-(trifluoromethyl)benzoate

Guidance literature:: Multi-step reaction with 3 steps

1.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 1 h

1.2: 18 h

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

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

With bis-triphenylphosphine-palladium(II) chloride; N-Bromosuccinimide; tetrabutylammomium bromide; 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

: 1442425-35-5
methyl 3-(1-(cyclohexylmethyl)-5-methyl-4-(oxetan-3-ylcarbamoyl)-1H-pyrrol-2-yl)-5-(trifluoromethyl)benzoate

Guidance literature:: Multi-step reaction with 2 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

With bis-triphenylphosphine-palladium(II) chloride; N-Bromosuccinimide; tetrabutylammomium bromide; potassium carbonate; In tetrahydrofuran; 1,4-dioxane; water;