(R)-N-(4-chlorophenylethyl)-1-(5-fluoropyrimidin-2-yl)piperidine-3-carboxamide

Base Information

Chemical Name:(R)-N-(4-chlorophenylethyl)-1-(5-fluoropyrimidin-2-yl)piperidine-3-carboxamide
CAS No.:1595144-17-4
Molecular Formula:C₁₈H₂₀ClFN₄O
Molecular Weight:362.834
Hs Code.:

Synonyms:(R)-N-(4-chlorophenylethyl)-1-(5-fluoropyrimidin-2-yl)piperidine-3-carboxamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (R)-N-(4-chlorophenylethyl)-1-(5-fluoropyrimidin-2-yl)piperidine-3-carboxamide

Chemical Property:

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Technology Process of (R)-N-(4-chlorophenylethyl)-1-(5-fluoropyrimidin-2-yl)piperidine-3-carboxamide

There total 4 articles about (R)-N-(4-chlorophenylethyl)-1-(5-fluoropyrimidin-2-yl)piperidine-3-carboxamide 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: 69.0%

: 1595143-76-2
(R)-N-(4-chlorophenylethyl)piperidine-3-carboxamide 2,2,2-trifluoroacetate

: 62802-42-0
2-chloro-5-fluoropyrimidine

: 1595144-17-4
(R)-N-(4-chlorophenylethyl)-1-(5-fluoropyrimidin-2-yl)piperidine-3-carboxamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In isopropyl alcohol; at 100 ℃; for 2h; Sealed tube;
DOI:10.1021/jm401731q

Reference yield:

: 163438-09-3
(R)-1-Boc-nipecotic acid

: 1595144-17-4
(R)-N-(4-chlorophenylethyl)-1-(5-fluoropyrimidin-2-yl)piperidine-3-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / acetonitrile / 25 °C

2: dichloromethane / 1 h

3: N-ethyl-N,N-diisopropylamine / isopropyl alcohol / 2 h / 100 °C / Sealed tube

With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In dichloromethane; isopropyl alcohol; acetonitrile;
DOI:10.1021/jm401731q

Reference yield:

: 1595143-73-9
C₁₉H₂₇ClN₂O₃

: 1595144-17-4
(R)-N-(4-chlorophenylethyl)-1-(5-fluoropyrimidin-2-yl)piperidine-3-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: dichloromethane / 1 h

2: N-ethyl-N,N-diisopropylamine / isopropyl alcohol / 2 h / 100 °C / Sealed tube

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