[5-(2-{4-[2-(trifluoromethyl)benzoyl]piperidin-1-yl}pyrimidin-5-yl)-2H-tetrazol-2-yl]acetic acid

Base Information

Chemical Name:[5-(2-{4-[2-(trifluoromethyl)benzoyl]piperidin-1-yl}pyrimidin-5-yl)-2H-tetrazol-2-yl]acetic acid
CAS No.:1241896-60-5
Molecular Formula:C₂₀H₁₈F₃N₇O₃
Molecular Weight:461.403
Hs Code.:

Synonyms:[5-(2-{4-[2-(trifluoromethyl)benzoyl]piperidin-1-yl}pyrimidin-5-yl)-2H-tetrazol-2-yl]acetic acid

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Chemical Property of [5-(2-{4-[2-(trifluoromethyl)benzoyl]piperidin-1-yl}pyrimidin-5-yl)-2H-tetrazol-2-yl]acetic acid

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Technology Process of [5-(2-{4-[2-(trifluoromethyl)benzoyl]piperidin-1-yl}pyrimidin-5-yl)-2H-tetrazol-2-yl]acetic acid

There total 6 articles about [5-(2-{4-[2-(trifluoromethyl)benzoyl]piperidin-1-yl}pyrimidin-5-yl)-2H-tetrazol-2-yl]acetic 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:

: ethyl [5-(2-{4-[2-(trifluoromethyl)benzoyl]piperidin-1-yl}pyrimidin-5-yl)-2H-tetrazol-2-yl]acetate

: 1241896-60-5
[5-(2-{4-[2-(trifluoromethyl)benzoyl]piperidin-1-yl}pyrimidin-5-yl)-2H-tetrazol-2-yl]acetic acid

Guidance literature:: With water; lithium hydroxide; In methanol; at 20 ℃; for 16h;

Reference yield:

: 1241898-02-1
ethyl [5-(2-aminopyrimidin-5-yl)-2H-tetrazol-2-yl]acetate

: 1241896-60-5
[5-(2-{4-[2-(trifluoromethyl)benzoyl]piperidin-1-yl}pyrimidin-5-yl)-2H-tetrazol-2-yl]acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1: tert.-butylnitrite; antimony(III) chloride / ethyl acetate; 1,2-dichloro-ethane / 3.25 h / 0 °C

2: potassium carbonate / 1,4-dioxane; dimethyl sulfoxide / 18 h / 70 °C

3: water; lithium hydroxide / 1,4-dioxane; methanol / 16 h / 20 °C

With tert.-butylnitrite; water; antimony(III) chloride; potassium carbonate; lithium hydroxide; In 1,4-dioxane; methanol; dimethyl sulfoxide; ethyl acetate; 1,2-dichloro-ethane;

Reference yield:

: 1241897-98-2
2-(benzylamino)pyrimidine-5-carbonitrile

: 1241896-60-5
[5-(2-{4-[2-(trifluoromethyl)benzoyl]piperidin-1-yl}pyrimidin-5-yl)-2H-tetrazol-2-yl]acetic acid

Guidance literature:: Multi-step reaction with 6 steps

1: sodium azide; ammonium chloride / N,N-dimethyl-formamide / 5 h / 100 °C / Inert atmosphere

2: triethylamine / tetrahydrofuran / 1 h / 65 °C

3: ammonium cerium (IV) nitrate / acetonitrile; water / 1.25 h / 20 °C

4: tert.-butylnitrite; antimony(III) chloride / ethyl acetate; 1,2-dichloro-ethane / 3.25 h / 0 °C

5: potassium carbonate / 1,4-dioxane; dimethyl sulfoxide / 18 h / 70 °C

6: water; lithium hydroxide / 1,4-dioxane; methanol / 16 h / 20 °C

With sodium azide; tert.-butylnitrite; ammonium cerium (IV) nitrate; water; antimony(III) chloride; potassium carbonate; ammonium chloride; triethylamine; lithium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; water; dimethyl sulfoxide; ethyl acetate; 1,2-dichloro-ethane; N,N-dimethyl-formamide; acetonitrile;