(3S)-1-[5-(3-{[2-(difluoromethoxy)phenyl]methyl}-2,7-dimethylimidazo[1,2-a]pyridin-6-yl)pyrimidin-2-yl]piperidine-3-carboxylic acid

Base Information

Chemical Name:(3S)-1-[5-(3-{[2-(difluoromethoxy)phenyl]methyl}-2,7-dimethylimidazo[1,2-a]pyridin-6-yl)pyrimidin-2-yl]piperidine-3-carboxylic acid
CAS No.:1536381-00-6
Molecular Formula:C₂₇H₂₇F₂N₅O₃
Molecular Weight:507.54
Hs Code.:

Synonyms:(3S)-1-[5-(3-{[2-(difluoromethoxy)phenyl]methyl}-2,7-dimethylimidazo[1,2-a]pyridin-6-yl)pyrimidin-2-yl]piperidine-3-carboxylic acid

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Chemical Property of (3S)-1-[5-(3-{[2-(difluoromethoxy)phenyl]methyl}-2,7-dimethylimidazo[1,2-a]pyridin-6-yl)pyrimidin-2-yl]piperidine-3-carboxylic acid

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Technology Process of (3S)-1-[5-(3-{[2-(difluoromethoxy)phenyl]methyl}-2,7-dimethylimidazo[1,2-a]pyridin-6-yl)pyrimidin-2-yl]piperidine-3-carboxylic acid

There total 2 articles about (3S)-1-[5-(3-{[2-(difluoromethoxy)phenyl]methyl}-2,7-dimethylimidazo[1,2-a]pyridin-6-yl)pyrimidin-2-yl]piperidine-3-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: 18.0%

: 1536391-31-7
2-chloro-5-{3-[2-(difluoromethoxy)benzyl]-2,7-dimethylimidazo[1,2-a]pyridin-6-yl}-pyrimidine

: 498-95-3,25137-00-2,59045-82-8,60252-41-7,262853-93-0
(S)-nipecotic acid

: 1536381-00-6
(3S)-1-[5-(3-{[2-(difluoromethoxy)phenyl]methyl}-2,7-dimethylimidazo[1,2-a]pyridin-6-yl)pyrimidin-2-yl]piperidine-3-carboxylic acid

Guidance literature:: With triethylamine; N-ethyl-N,N-diisopropylamine; In 1-methyl-pyrrolidin-2-one; at 100 ℃; for 3h; Sealed tube; Inert atmosphere;

Reference yield:

: 98198-48-2
2-amino-5-bromo-4-methylpyridine

: 1536381-00-6
(3S)-1-[5-(3-{[2-(difluoromethoxy)phenyl]methyl}-2,7-dimethylimidazo[1,2-a]pyridin-6-yl)pyrimidin-2-yl]piperidine-3-carboxylic acid

Guidance literature:: Multi-step reaction with 6 steps

1: methanol / 16 h / 80 °C

2: toluene / 1.67 h / 100 °C

3: sodium tetrahydroborate; methanol / 1.25 h / 0 °C

4: triethylsilane; boron trifluoride diethyl etherate / 20 h / 20 °C / Inert atmosphere

5: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; sodium carbonate; tri-tert-butyl phosphine / 1,4-dioxane; water / 1 h / 110 - 120 °C / Inert atmosphere

6: triethylamine; N-ethyl-N,N-diisopropylamine / 1-methyl-pyrrolidin-2-one / 3 h / 100 °C / Sealed tube; Inert atmosphere

With methanol; triethylsilane; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; sodium tetrahydroborate; tri-tert-butyl phosphine; boron trifluoride diethyl etherate; sodium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; 1-methyl-pyrrolidin-2-one; methanol; water; toluene;