(R)-ethyl 1-(6-(3-((4-cyanophenylethyl)carbamoyl)piperidin-1-yl)-2-(trifluoromethyl)pyrimidin-4-yl)piperidine-4-carboxylate

Base Information

Chemical Name:(R)-ethyl 1-(6-(3-((4-cyanophenylethyl)carbamoyl)piperidin-1-yl)-2-(trifluoromethyl)pyrimidin-4-yl)piperidine-4-carboxylate
CAS No.:1595145-12-2
Molecular Formula:C₂₈H₃₃F₃N₆O₃
Molecular Weight:558.604
Hs Code.:

Synonyms:(R)-ethyl 1-(6-(3-((4-cyanophenylethyl)carbamoyl)piperidin-1-yl)-2-(trifluoromethyl)pyrimidin-4-yl)piperidine-4-carboxylate

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Chemical Property of (R)-ethyl 1-(6-(3-((4-cyanophenylethyl)carbamoyl)piperidin-1-yl)-2-(trifluoromethyl)pyrimidin-4-yl)piperidine-4-carboxylate

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Technology Process of (R)-ethyl 1-(6-(3-((4-cyanophenylethyl)carbamoyl)piperidin-1-yl)-2-(trifluoromethyl)pyrimidin-4-yl)piperidine-4-carboxylate

There total 7 articles about (R)-ethyl 1-(6-(3-((4-cyanophenylethyl)carbamoyl)piperidin-1-yl)-2-(trifluoromethyl)pyrimidin-4-yl)piperidine-4-carboxylate 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: 85.0%

: 1126-09-6
4-carbethoxypiperidine

: 1595144-50-5
(R)-1-(6-chloro-2-(trifluoromethyl)pyrimidin-4-yl)-N-(4-cyanophenylethyl)piperidine-3-carboxamide

: 1595145-12-2
(R)-ethyl 1-(6-(3-((4-cyanophenylethyl)carbamoyl)piperidin-1-yl)-2-(trifluoromethyl)pyrimidin-4-yl)piperidine-4-carboxylate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In isopropyl alcohol; at 130 ℃; for 20h; Sealed tube;
DOI:10.1021/jm401731q

Reference yield:

: 1595144-08-3
(R)-tert-butyl 3-((4-cyanophenylethyl)carbamoyl)piperidine-1-carboxylate

: 1595145-12-2
(R)-ethyl 1-(6-(3-((4-cyanophenylethyl)carbamoyl)piperidin-1-yl)-2-(trifluoromethyl)pyrimidin-4-yl)piperidine-4-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: hydrogenchloride / ethyl acetate; 1,4-dioxane / 0 °C

1.2: pH 12

2.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 0.5 h / 0 - 25 °C

3.1: N-ethyl-N,N-diisopropylamine / isopropyl alcohol / 20 h / 130 °C / Sealed tube

With hydrogenchloride; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; ethyl acetate; isopropyl alcohol; acetonitrile;
DOI:10.1021/jm401731q

Reference yield:

: 1595144-10-7
C₁₅H₁₉N₃O*ClH

: 1595145-12-2
(R)-ethyl 1-(6-(3-((4-cyanophenylethyl)carbamoyl)piperidin-1-yl)-2-(trifluoromethyl)pyrimidin-4-yl)piperidine-4-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: N-ethyl-N,N-diisopropylamine / isopropyl alcohol / 0.25 h / 0 - 25 °C

2: N-ethyl-N,N-diisopropylamine / isopropyl alcohol / 20 h / 130 °C / Sealed tube

With N-ethyl-N,N-diisopropylamine; In isopropyl alcohol;
DOI:10.1021/jm401731q