1-benzyl-4-[N-methyl-N-(3-(cyclopropylamino)-2-pyridinyl)amino]piperidine

Base Information

Chemical Name:1-benzyl-4-[N-methyl-N-(3-(cyclopropylamino)-2-pyridinyl)amino]piperidine
CAS No.:179557-29-0
Molecular Formula:C₂₁H₂₈N₄
Molecular Weight:336.48
Hs Code.:

Synonyms:1-benzyl-4-[N-methyl-N-(3-(cyclopropylamino)-2-pyridinyl)amino]piperidine

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Chemical Property of 1-benzyl-4-[N-methyl-N-(3-(cyclopropylamino)-2-pyridinyl)amino]piperidine

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Technology Process of 1-benzyl-4-[N-methyl-N-(3-(cyclopropylamino)-2-pyridinyl)amino]piperidine

There total 6 articles about 1-benzyl-4-[N-methyl-N-(3-(cyclopropylamino)-2-pyridinyl)amino]piperidine 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: 59.0%

: 179557-28-9
1-benzyl-4-[N-methyl-N-(3-(1-ethoxycyclopropylamino)-2-pyridinyl)amino]piperidine

: 179557-29-0
1-benzyl-4-[N-methyl-N-(3-(cyclopropylamino)-2-pyridinyl)amino]piperidine

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; for 1h; Ambient temperature;
DOI:10.1021/jm960158n

Reference yield:

: 5470-18-8,34515-82-7
2-Chloro-3-nitropyridine

: 179557-29-0
1-benzyl-4-[N-methyl-N-(3-(cyclopropylamino)-2-pyridinyl)amino]piperidine

Guidance literature:: Multi-step reaction with 4 steps

1: 95 percent / K₂CO₃ / acetonitrile / 120 h / Ambient temperature

2: 100 percent / TiCl₃, aq. HCl / 21 h / Ambient temperature

3: triethylamine / tetrahydrofuran / 48 h / Heating

4: 59 percent / lithium aluminum hydride / tetrahydrofuran / 1 h / Ambient temperature

With hydrogenchloride; lithium aluminium tetrahydride; titanium(III) chloride; potassium carbonate; triethylamine; In tetrahydrofuran; acetonitrile;
DOI:10.1021/jm960158n

Reference yield:

: 3612-20-2
1-phenylmethyl-4-piperidone

: 179557-29-0
1-benzyl-4-[N-methyl-N-(3-(cyclopropylamino)-2-pyridinyl)amino]piperidine

Guidance literature:: Multi-step reaction with 5 steps

1: 76 percent / sodium cyanoborohydride, 4 Angstroem molecular sieves / methanol / 24 h / Ambient temperature

2: 95 percent / K₂CO₃ / acetonitrile / 120 h / Ambient temperature

3: 100 percent / TiCl₃, aq. HCl / 21 h / Ambient temperature

4: triethylamine / tetrahydrofuran / 48 h / Heating

5: 59 percent / lithium aluminum hydride / tetrahydrofuran / 1 h / Ambient temperature

With hydrogenchloride; lithium aluminium tetrahydride; titanium(III) chloride; 4 A molecular sieve; sodium cyanoborohydride; potassium carbonate; triethylamine; In tetrahydrofuran; methanol; acetonitrile;
DOI:10.1021/jm960158n