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

Base Information

Chemical Name:2-{[(3R,6R)-6-methyl-1-{[2-(2H-1,2,3-triazol-2-yl)phenyl]carbonyl}piperidin-3-yl]oxy}pyridine-4-carboxylic acid
CAS No.:1616262-57-7
Molecular Formula:C₂₁H₂₁N₅O₄
Molecular Weight:407.429
Hs Code.:

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

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

Chemical Property:

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

There total 21 articles about 2-{[(3R,6R)-6-methyl-1-{[2-(2H-1,2,3-triazol-2-yl)phenyl]carbonyl}piperidin-3-yl]oxy}pyridine-4-carboxylic acid 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:

: 774238-83-4
2-fluoro-N-methyl-N-(methyloxy)-4-pyridinecarboxamide

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

: 1616262-57-7
2-{[(3R,6R)-6-methyl-1-{[2-(2H-1,2,3-triazol-2-yl)phenyl]carbonyl}piperidin-3-yl]oxy}pyridine-4-carboxylic acid

Guidance literature:: (2-(2H-1,2,3-triazol-2-yl)phenyl)((2R,5R)-5-hydroxy-2-methylpiperidin-1-yl)methanone; With sodium hydride; In N,N-dimethyl-formamide; at 0 ℃; for 0.5h;

2-fluoro-N-methyl-N-(methyloxy)-4-pyridinecarboxamide; In N,N-dimethyl-formamide; at 20 ℃; for 12h;

Reference yield:

: 58481-11-1
methyl 2-chloroisonicotinate

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

: 1616262-56-6
methyl 2-{[(3R,6R)-6-methyl-1-{[2-(2H-1,2,3-triazol-2-yl)phenyl]carbonyl}piperidin-3-yl]oxy}pyridine-4-carboxylate

: 1616262-57-7
2-{[(3R,6R)-6-methyl-1-{[2-(2H-1,2,3-triazol-2-yl)phenyl]carbonyl}piperidin-3-yl]oxy}pyridine-4-carboxylic acid

Guidance literature:: (2-(2H-1,2,3-triazol-2-yl)phenyl)((2R,5R)-5-hydroxy-2-methylpiperidin-1-yl)methanone; With sodium hydride; In N,N-dimethyl-formamide; for 0.0833333h;

methyl 2-chloroisonicotinate; In N,N-dimethyl-formamide; at 50 - 120 ℃;

With hydrogenchloride; In N,N-dimethyl-formamide; at 20 ℃;

Reference yield:

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

: 1616262-57-7
2-{[(3R,6R)-6-methyl-1-{[2-(2H-1,2,3-triazol-2-yl)phenyl]carbonyl}piperidin-3-yl]oxy}pyridine-4-carboxylic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: 4-(N,N-Dimethylamino)triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / -25 - 20 °C / Inert atmosphere

2.1: sodium hydroxide; water / methanol; tetrahydrofuran

3.1: hydrogen; palladium 10% on activated carbon / ethanol / 72 h

4.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; 1-hydroxy-7-aza-benzotriazole; triethylamine / N,N-dimethyl-formamide / 50 °C

5.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 0 °C

5.2: 12 h / 20 °C

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