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

Base Information

Chemical Name:1-benzyl-4-[N-methyl-N-(3-(1-methylcyclopropylamino)-2-pyridinyl)amino]piperidine
CAS No.:179557-31-4
Molecular Formula:C₂₂H₃₀N₄
Molecular Weight:350.507
Hs Code.:

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

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

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

There total 7 articles about 1-benzyl-4-[N-methyl-N-(3-(1-methylcyclopropylamino)-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: 78.0%

: 917-54-4
methyllithium

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

: 179557-31-4
1-benzyl-4-[N-methyl-N-(3-(1-methylcyclopropylamino)-2-pyridinyl)amino]piperidine

Guidance literature:: With lithium bromide; In diethyl ether; toluene; at -78 ℃; for 1h;
DOI:10.1021/jm960158n

Reference yield:

: methyllithium lithium bromide

: 71086-99-2
ethyl 5-amino-1H-indole-2-carboxylate

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

: 179557-31-4
1-benzyl-4-[N-methyl-N-(3-(1-methylcyclopropylamino)-2-pyridinyl)amino]piperidine

Guidance literature:: In toluene;

Reference yield:

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

: 179557-31-4
1-benzyl-4-[N-methyl-N-(3-(1-methylcyclopropylamino)-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: 78 percent / LiBr / toluene; diethyl ether / 1 h / -78 °C

With hydrogenchloride; titanium(III) chloride; potassium carbonate; triethylamine; lithium bromide; In tetrahydrofuran; diethyl ether; toluene; acetonitrile;
DOI:10.1021/jm960158n