3-(4-(5-chloropyridin-3-yl)-3-(((trans)-4-methylcyclohexyl)methyl)-2-((S)-2-(trifluoromethyl)pyrrolidin-1-yl)-3H-imidazo[4,5-c]pyridin-6-yl)-1,2,4-oxadiazol-5(4H)-one

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Chemical Name:3-(4-(5-chloropyridin-3-yl)-3-(((trans)-4-methylcyclohexyl)methyl)-2-((S)-2-(trifluoromethyl)pyrrolidin-1-yl)-3H-imidazo[4,5-c]pyridin-6-yl)-1,2,4-oxadiazol-5(4H)-one
CAS No.:1616428-81-9
Molecular Formula:C₂₆H₂₇ClF₃N₇O₂
Molecular Weight:561.994
Hs Code.:

3-(4-(5-chloropyridin-3-yl)-3-(((trans)-4-methylcyclohexyl)methyl)-2-((S)-2-(trifluoromethyl)pyrrolidin-1-yl)-3H-imidazo[4,5-c]pyridin-6-yl)-1,2,4-oxadiazol-5(4H)-one

Synonyms:3-(4-(5-chloropyridin-3-yl)-3-(((trans)-4-methylcyclohexyl)methyl)-2-((S)-2-(trifluoromethyl)pyrrolidin-1-yl)-3H-imidazo[4,5-c]pyridin-6-yl)-1,2,4-oxadiazol-5(4H)-one

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Chemical Property of 3-(4-(5-chloropyridin-3-yl)-3-(((trans)-4-methylcyclohexyl)methyl)-2-((S)-2-(trifluoromethyl)pyrrolidin-1-yl)-3H-imidazo[4,5-c]pyridin-6-yl)-1,2,4-oxadiazol-5(4H)-one

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Technology Process of 3-(4-(5-chloropyridin-3-yl)-3-(((trans)-4-methylcyclohexyl)methyl)-2-((S)-2-(trifluoromethyl)pyrrolidin-1-yl)-3H-imidazo[4,5-c]pyridin-6-yl)-1,2,4-oxadiazol-5(4H)-one

There total 21 articles about 3-(4-(5-chloropyridin-3-yl)-3-(((trans)-4-methylcyclohexyl)methyl)-2-((S)-2-(trifluoromethyl)pyrrolidin-1-yl)-3H-imidazo[4,5-c]pyridin-6-yl)-1,2,4-oxadiazol-5(4H)-one 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: 82.0%

: 1616435-04-1
4-(5-chloropyridin-3-yl)-N'-hydroxy-3-[(trans-4-methylcyclohexyl)methyl]-2-[(2S)-2-(trifluoromethyl)pyrrolidin-1-yl]-3H-imidazo[4,5-c]pyridine-6-carboximidamide

: 530-62-1
1,1'-carbonyldiimidazole

: 1616428-81-9
3-(4-(5-chloropyridin-3-yl)-3-(((trans)-4-methylcyclohexyl)methyl)-2-((S)-2-(trifluoromethyl)pyrrolidin-1-yl)-3H-imidazo[4,5-c]pyridin-6-yl)-1,2,4-oxadiazol-5(4H)-one

Guidance literature:: With 1,8-diazabicyclo[5.4.0]undec-7-ene; In acetonitrile; at 20 ℃; for 1h;
DOI:10.1021/acs.jmedchem.1c01524

Reference yield:

: 1616434-24-2
4,6-dichloro-3-(((trans)-4-methylcyclohexyl)methyl)-3H-imidazo[4,5-c]pyridine

: 1616428-81-9
3-(4-(5-chloropyridin-3-yl)-3-(((trans)-4-methylcyclohexyl)methyl)-2-((S)-2-(trifluoromethyl)pyrrolidin-1-yl)-3H-imidazo[4,5-c]pyridin-6-yl)-1,2,4-oxadiazol-5(4H)-one

Guidance literature:: Multi-step reaction with 6 steps

1: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; caesium carbonate / 1,4-dioxane; water / 3 h / 90 °C / Inert atmosphere; Sealed tube

2: (R)-2,2'-bis(diphenylphosphanyl)-1,1'-binaphthyl; zinc; palladium diacetate; sulfuric acid / N,N-dimethyl acetamide / 3.5 h / 100 °C / Inert atmosphere

3: N-Bromosuccinimide / chloroform / 1 h / Reflux

4: N-ethyl-N,N-diisopropylamine; potassium fluoride / dimethyl sulfoxide / 16 h / 100 °C / Sealed tube

5: hydroxylamine hydrochloride; sodium hydrogencarbonate / water; ethanol / 1 h / 100 °C

6: 1,8-diazabicyclo[5.4.0]undec-7-ene / acetonitrile / 1 h / 20 °C

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium fluoride; N-Bromosuccinimide; sulfuric acid; hydroxylamine hydrochloride; palladium diacetate; sodium hydrogencarbonate; caesium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; (R)-2,2'-bis(diphenylphosphanyl)-1,1'-binaphthyl; N-ethyl-N,N-diisopropylamine; zinc; In 1,4-dioxane; ethanol; chloroform; N,N-dimethyl acetamide; water; dimethyl sulfoxide; acetonitrile;

Reference yield:

: 1616434-29-7
6-chloro-4-(5-chloropyridin-3-yl)-3-(((trans)-4-methylcyclohexyl)methyl)-3H-imidazo[4,5-c]pyridine

: 1616428-81-9
3-(4-(5-chloropyridin-3-yl)-3-(((trans)-4-methylcyclohexyl)methyl)-2-((S)-2-(trifluoromethyl)pyrrolidin-1-yl)-3H-imidazo[4,5-c]pyridin-6-yl)-1,2,4-oxadiazol-5(4H)-one

Guidance literature:: Multi-step reaction with 5 steps

1: (R)-2,2'-bis(diphenylphosphanyl)-1,1'-binaphthyl; zinc; palladium diacetate; sulfuric acid / N,N-dimethyl acetamide / 3.5 h / 100 °C / Inert atmosphere

2: N-Bromosuccinimide / chloroform / 1 h / Reflux

3: N-ethyl-N,N-diisopropylamine; potassium fluoride / dimethyl sulfoxide / 16 h / 100 °C / Sealed tube

4: hydroxylamine hydrochloride; sodium hydrogencarbonate / water; ethanol / 1 h / 100 °C

5: 1,8-diazabicyclo[5.4.0]undec-7-ene / acetonitrile / 1 h / 20 °C

With potassium fluoride; N-Bromosuccinimide; sulfuric acid; hydroxylamine hydrochloride; palladium diacetate; sodium hydrogencarbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; (R)-2,2'-bis(diphenylphosphanyl)-1,1'-binaphthyl; N-ethyl-N,N-diisopropylamine; zinc; In ethanol; chloroform; N,N-dimethyl acetamide; water; dimethyl sulfoxide; acetonitrile;