4-(methylsulfanyl)-2-{[(3R,6R)-6-methyl-1-{[2-(2H-1,2,3-triazol-2-yl)phenyl]carbonyl}piperidin-3-yl]oxy}pyridine-3-carbonitrile

Base Information

Chemical Name:4-(methylsulfanyl)-2-{[(3R,6R)-6-methyl-1-{[2-(2H-1,2,3-triazol-2-yl)phenyl]carbonyl}piperidin-3-yl]oxy}pyridine-3-carbonitrile
CAS No.:1616373-56-8
Molecular Formula:C₂₂H₂₂N₆O₂S
Molecular Weight:434.522
Hs Code.:

Synonyms:4-(methylsulfanyl)-2-{[(3R,6R)-6-methyl-1-{[2-(2H-1,2,3-triazol-2-yl)phenyl]carbonyl}piperidin-3-yl]oxy}pyridine-3-carbonitrile

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Chemical Property of 4-(methylsulfanyl)-2-{[(3R,6R)-6-methyl-1-{[2-(2H-1,2,3-triazol-2-yl)phenyl]carbonyl}piperidin-3-yl]oxy}pyridine-3-carbonitrile

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Technology Process of 4-(methylsulfanyl)-2-{[(3R,6R)-6-methyl-1-{[2-(2H-1,2,3-triazol-2-yl)phenyl]carbonyl}piperidin-3-yl]oxy}pyridine-3-carbonitrile

There total 7 articles about 4-(methylsulfanyl)-2-{[(3R,6R)-6-methyl-1-{[2-(2H-1,2,3-triazol-2-yl)phenyl]carbonyl}piperidin-3-yl]oxy}pyridine-3-carbonitrile 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:

: 1257072-10-8
2-chloro-4-(methylthio)nicotinonitrile

: 1222491-34-0
(2-(2H-1,2,3-triazol-2-yl)phenyl)((2R,5R)-5-hydroxy-2-methylpiperidin-1-yl)methanone

: 1616373-56-8
4-(methylsulfanyl)-2-{[(3R,6R)-6-methyl-1-{[2-(2H-1,2,3-triazol-2-yl)phenyl]carbonyl}piperidin-3-yl]oxy}pyridine-3-carbonitrile

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide; at 50 ℃; for 96h;

Reference yield:

: 1431473-03-8
benzyl (2R,5R)-2-methyl-5-{[(4-nitrophenyl)carbonyl]oxy}piperidine-1-carboxylate

: 1616373-56-8
4-(methylsulfanyl)-2-{[(3R,6R)-6-methyl-1-{[2-(2H-1,2,3-triazol-2-yl)phenyl]carbonyl}piperidin-3-yl]oxy}pyridine-3-carbonitrile

Guidance literature:: Multi-step reaction with 4 steps

1: sodium hydroxide / methanol; tetrahydrofuran; water

2: palladium 10% on activated carbon; hydrogen / ethanol

3: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; 1-hydroxy-7-aza-benzotriazole / N,N-dimethyl-formamide / 50 °C

4: sodium hydride / N,N-dimethyl-formamide / 96 h / 50 °C

With 1-hydroxy-7-aza-benzotriazole; palladium 10% on activated carbon; hydrogen; sodium hydride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; sodium hydroxide; In tetrahydrofuran; methanol; ethanol; water; N,N-dimethyl-formamide;

Reference yield:

: 1431473-24-3
(2R,5S)-benzyl 5-hydroxy-2-methylpiperidine-1-carboxylate

: 1616373-56-8
4-(methylsulfanyl)-2-{[(3R,6R)-6-methyl-1-{[2-(2H-1,2,3-triazol-2-yl)phenyl]carbonyl}piperidin-3-yl]oxy}pyridine-3-carbonitrile

Guidance literature:: Multi-step reaction with 5 steps

1: 4-(N,N-Dimethylamino)triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 0.33 h / -25 - 20 °C / Inert atmosphere

2: sodium hydroxide / methanol; tetrahydrofuran; water

3: palladium 10% on activated carbon; hydrogen / ethanol

4: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; 1-hydroxy-7-aza-benzotriazole / N,N-dimethyl-formamide / 50 °C

5: sodium hydride / N,N-dimethyl-formamide / 96 h / 50 °C

With 1-hydroxy-7-aza-benzotriazole; palladium 10% on activated carbon; hydrogen; sodium hydride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; sodium hydroxide; diethylazodicarboxylate; 4-(N,N-Dimethylamino)triphenylphosphine; In tetrahydrofuran; methanol; ethanol; water; N,N-dimethyl-formamide;