methyl 4-{2-[6-{[(2R)-2-isobutylpyrrolidin-1-yl]methyl}-2-oxo-3,5-bis[2-(trifluoromethoxy)phenyl]pyridin-1(2H)-yl]ethyl}benzoate

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Chemical Name:methyl 4-{2-[6-{[(2R)-2-isobutylpyrrolidin-1-yl]methyl}-2-oxo-3,5-bis[2-(trifluoromethoxy)phenyl]pyridin-1(2H)-yl]ethyl}benzoate
CAS No.:1201824-00-1
Molecular Formula:C₃₈H₃₈F₆N₂O₅
Molecular Weight:716.721
Hs Code.:

Synonyms:methyl 4-{2-[6-{[(2R)-2-isobutylpyrrolidin-1-yl]methyl}-2-oxo-3,5-bis[2-(trifluoromethoxy)phenyl]pyridin-1(2H)-yl]ethyl}benzoate

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Chemical Property of methyl 4-{2-[6-{[(2R)-2-isobutylpyrrolidin-1-yl]methyl}-2-oxo-3,5-bis[2-(trifluoromethoxy)phenyl]pyridin-1(2H)-yl]ethyl}benzoate

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Technology Process of methyl 4-{2-[6-{[(2R)-2-isobutylpyrrolidin-1-yl]methyl}-2-oxo-3,5-bis[2-(trifluoromethoxy)phenyl]pyridin-1(2H)-yl]ethyl}benzoate

There total 5 articles about methyl 4-{2-[6-{[(2R)-2-isobutylpyrrolidin-1-yl]methyl}-2-oxo-3,5-bis[2-(trifluoromethoxy)phenyl]pyridin-1(2H)-yl]ethyl}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:

: 1201824-07-8,1184994-37-3
(2R)-2-isobutylpyrrolidine monohydrochloride

: 1201823-98-4
methyl 4-{2-[6-(bromomethyl)-2-oxo-3,5-bis[2-(trifluoromethoxy)phenyl]pyridin-1(2H)-yl]ethyl}benzoate

: 1201824-00-1
methyl 4-{2-[6-{[(2R)-2-isobutylpyrrolidin-1-yl]methyl}-2-oxo-3,5-bis[2-(trifluoromethoxy)phenyl]pyridin-1(2H)-yl]ethyl}benzoate

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃;

Reference yield:

: 1091599-76-6
methyl 4-[2-(5-bromo-3-chloro-6-methyl-2-oxopyridin-1(2H)-yl)ethyl]benzoate

: 1201824-00-1
methyl 4-{2-[6-{[(2R)-2-isobutylpyrrolidin-1-yl]methyl}-2-oxo-3,5-bis[2-(trifluoromethoxy)phenyl]pyridin-1(2H)-yl]ethyl}benzoate

Guidance literature:: Multi-step reaction with 3 steps

1: potassium phosphate; dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane / palladium diacetate / ethyl acetate; toluene; water / 90 °C

2: 2,2'-azobis(isobutyronitrile); N-Bromosuccinimide / tetrachloromethane / Heating; Reflux

3: potassium carbonate / N,N-dimethyl-formamide / 20 °C

With dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; potassium phosphate; N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); potassium carbonate; palladium diacetate; In tetrachloromethane; water; ethyl acetate; N,N-dimethyl-formamide; toluene;

Reference yield:

: 1201823-01-9
methyl 4-[2-(3-chloro-6-methyl-2-oxopyridin-1(2H)-yl)ethyl]benzoate

: 1201824-00-1
methyl 4-{2-[6-{[(2R)-2-isobutylpyrrolidin-1-yl]methyl}-2-oxo-3,5-bis[2-(trifluoromethoxy)phenyl]pyridin-1(2H)-yl]ethyl}benzoate

Guidance literature:: Multi-step reaction with 4 steps

1: N-Bromosuccinimide; acetic acid / water / 20 °C

2: potassium phosphate; dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane / palladium diacetate / ethyl acetate; toluene; water / 90 °C

3: 2,2'-azobis(isobutyronitrile); N-Bromosuccinimide / tetrachloromethane / Heating; Reflux

4: potassium carbonate / N,N-dimethyl-formamide / 20 °C

With dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; potassium phosphate; N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); potassium carbonate; acetic acid; palladium diacetate; In tetrachloromethane; water; ethyl acetate; N,N-dimethyl-formamide; toluene;