(3R,4E)-3-methyl-N-pyridin-3-yl-4-(3-{[5-(trifluoromethyl)pyrimidin-2-yl]oxy}benzylidene)piperidine-1-carboxamide

Base Information

Chemical Name:(3R,4E)-3-methyl-N-pyridin-3-yl-4-(3-{[5-(trifluoromethyl)pyrimidin-2-yl]oxy}benzylidene)piperidine-1-carboxamide
CAS No.:1191286-54-0
Molecular Formula:C₂₄H₂₂F₃N₅O₂
Molecular Weight:469.466
Hs Code.:

Synonyms:(3R,4E)-3-methyl-N-pyridin-3-yl-4-(3-{[5-(trifluoromethyl)pyrimidin-2-yl]oxy}benzylidene)piperidine-1-carboxamide

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Chemical Property of (3R,4E)-3-methyl-N-pyridin-3-yl-4-(3-{[5-(trifluoromethyl)pyrimidin-2-yl]oxy}benzylidene)piperidine-1-carboxamide

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Technology Process of (3R,4E)-3-methyl-N-pyridin-3-yl-4-(3-{[5-(trifluoromethyl)pyrimidin-2-yl]oxy}benzylidene)piperidine-1-carboxamide

There total 8 articles about (3R,4E)-3-methyl-N-pyridin-3-yl-4-(3-{[5-(trifluoromethyl)pyrimidin-2-yl]oxy}benzylidene)piperidine-1-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:

: 1190843-58-3
tert-butyl 4-(3-hydroxybenzylidene)-3-methylpiperidine-1-carboxylate

: 69034-12-4,176214-12-3
5-(trifluoromethyl)pyrimidine

: 1191286-55-1
(3S,4E)-3-methyl-N-pyridin-3-yl-4-(3-{[5-(trifluoromethyl)pyrimidin-2-yl]oxy}benzylidene)piperidine-1-carboxamide

: 1191286-54-0
(3R,4E)-3-methyl-N-pyridin-3-yl-4-(3-{[5-(trifluoromethyl)pyrimidin-2-yl]oxy}benzylidene)piperidine-1-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: caesium carbonate / dimethyl sulfoxide / 1 h / 65 °C

1.2: 1 h / 20 °C

2.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 0.5 h

2.2: Chiralpak AD-H / Resolution of racemate

With caesium carbonate; N-ethyl-N,N-diisopropylamine; In dimethyl sulfoxide; acetonitrile;

Reference yield:

: 462-08-8
pyridin-3-ylamine

: 1191286-55-1
(3S,4E)-3-methyl-N-pyridin-3-yl-4-(3-{[5-(trifluoromethyl)pyrimidin-2-yl]oxy}benzylidene)piperidine-1-carboxamide

: 1191286-54-0
(3R,4E)-3-methyl-N-pyridin-3-yl-4-(3-{[5-(trifluoromethyl)pyrimidin-2-yl]oxy}benzylidene)piperidine-1-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: pyridine / tetrahydrofuran / 0.17 h / -10 °C

1.2: -10 - 20 °C

2.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 0.5 h

2.2: Chiralpak AD-H / Resolution of racemate

With pyridine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; acetonitrile;

Reference yield:

: 1190843-65-2
3-(hydroxymethyl)phenyl pivalate

: 1191286-55-1
(3S,4E)-3-methyl-N-pyridin-3-yl-4-(3-{[5-(trifluoromethyl)pyrimidin-2-yl]oxy}benzylidene)piperidine-1-carboxamide

: 1191286-54-0
(3R,4E)-3-methyl-N-pyridin-3-yl-4-(3-{[5-(trifluoromethyl)pyrimidin-2-yl]oxy}benzylidene)piperidine-1-carboxamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: 1H-imidazole; bromine; triphenylphosphine / dichloromethane / 0 - 20 °C

2.1: 4 h / 150 °C

3.1: potassium tert-butylate / tetrahydrofuran / 2 h / 20 °C

4.1: lithium aluminium tetrahydride / tetrahydrofuran / 20 °C

5.1: caesium carbonate / dimethyl sulfoxide / 1 h / 65 °C

5.2: 1 h / 20 °C

6.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 0.5 h

6.2: Chiralpak AD-H / Resolution of racemate

With 1H-imidazole; lithium aluminium tetrahydride; potassium tert-butylate; bromine; caesium carbonate; N-ethyl-N,N-diisopropylamine; triphenylphosphine; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide; acetonitrile;