[8-(3,4-Difluoro-phenyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyridin-2-yl]-[1-(5-methyl-[1,3,4]oxadiazol-2-yl)-piperidin-4-yl]-amine

Base Information

Chemical Name:[8-(3,4-Difluoro-phenyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyridin-2-yl]-[1-(5-methyl-[1,3,4]oxadiazol-2-yl)-piperidin-4-yl]-amine
CAS No.:1329670-85-0
Molecular Formula:C₂₀H₂₃F₂N₇O
Molecular Weight:415.446
Hs Code.:

Synonyms:[8-(3,4-Difluoro-phenyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyridin-2-yl]-[1-(5-methyl-[1,3,4]oxadiazol-2-yl)-piperidin-4-yl]-amine

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Chemical Property of [8-(3,4-Difluoro-phenyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyridin-2-yl]-[1-(5-methyl-[1,3,4]oxadiazol-2-yl)-piperidin-4-yl]-amine

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Technology Process of [8-(3,4-Difluoro-phenyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyridin-2-yl]-[1-(5-methyl-[1,3,4]oxadiazol-2-yl)-piperidin-4-yl]-amine

There total 3 articles about [8-(3,4-Difluoro-phenyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyridin-2-yl]-[1-(5-methyl-[1,3,4]oxadiazol-2-yl)-piperidin-4-yl]-amine 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: 18.0%

: 1329672-49-2
1-(5-methyl-[1,3,4]oxadiazol-2-yl)-piperidin-4-one

: 1329672-79-8
8-(3,4-difluorophenyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyridin-2-amine

: 1329670-85-0
[8-(3,4-Difluoro-phenyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyridin-2-yl]-[1-(5-methyl-[1,3,4]oxadiazol-2-yl)-piperidin-4-yl]-amine

Guidance literature:: 1-(5-methyl-[1,3,4]oxadiazol-2-yl)-piperidin-4-one; 8-(3,4-difluorophenyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyridin-2-amine; With acetic acid; In toluene; Reflux;

With sodium tetrahydroborate; ethanol; In toluene; at 50 ℃; for 6h;

Reference yield:

: 1329672-48-1
4-hydroxy-1-(5-methyl-[1,3,4]oxadiazol-2-yl)-1,2,5,6-tetrahydro-pyridine-3-carboxylic acid allyl ester potassium salt

: 1329670-85-0
[8-(3,4-Difluoro-phenyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyridin-2-yl]-[1-(5-methyl-[1,3,4]oxadiazol-2-yl)-piperidin-4-yl]-amine

Guidance literature:: Multi-step reaction with 2 steps

1.1: hydrogenchloride / water

1.2: 1.08 h / 20 °C / Inert atmosphere

2.1: acetic acid / toluene / Reflux

2.2: 6 h / 50 °C

With hydrogenchloride; acetic acid; In water; toluene;

Reference yield:

: 1329672-80-1
8-(3,4-difluoro-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine

: 1329670-85-0
[8-(3,4-Difluoro-phenyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyridin-2-yl]-[1-(5-methyl-[1,3,4]oxadiazol-2-yl)-piperidin-4-yl]-amine

Guidance literature:: Multi-step reaction with 2 steps

1.1: iodine; magnesium; methanol / tetrahydrofuran / 6.5 h / 20 - 50 °C

2.1: acetic acid / toluene / Reflux

2.2: 6 h / 50 °C

With methanol; iodine; magnesium; acetic acid; In tetrahydrofuran; toluene;