tert-butyl 4-methyl-4-(5-methyl-2-nitrophenylamino)piperidine-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-methyl-4-(5-methyl-2-nitrophenylamino)piperidine-1-carboxylate
CAS No.:1067188-65-1
Molecular Formula:C₁₈H₂₇N₃O₄
Molecular Weight:349.43
Hs Code.:

Synonyms:tert-butyl 4-methyl-4-(5-methyl-2-nitrophenylamino)piperidine-1-carboxylate

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Chemical Property of tert-butyl 4-methyl-4-(5-methyl-2-nitrophenylamino)piperidine-1-carboxylate

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Technology Process of tert-butyl 4-methyl-4-(5-methyl-2-nitrophenylamino)piperidine-1-carboxylate

There total 5 articles about tert-butyl 4-methyl-4-(5-methyl-2-nitrophenylamino)piperidine-1-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: 61.4%

: 446-34-4
2-fluoro-4-methyl-1-nitrobenzene

: 343788-69-2
4-amino-4-methyl-piperidine-1-carboxylic acid tert-butyl ester

: 1067188-65-1
tert-butyl 4-methyl-4-(5-methyl-2-nitrophenylamino)piperidine-1-carboxylate

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 20 - 110 ℃;

Reference yield:

: 163271-06-5
4-amino-1-benzyl-4-methylpiperidine

: 1067188-65-1
tert-butyl 4-methyl-4-(5-methyl-2-nitrophenylamino)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogen; acetic acid / palladium hydroxide on carbon / methanol / 20 °C / 2585.81 Torr

2: potassium carbonate / N,N-dimethyl-formamide / 20 - 110 °C

With hydrogen; potassium carbonate; acetic acid; palladium hydroxide on carbon; In methanol; N,N-dimethyl-formamide;

Reference yield:

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

: 1067188-65-1
tert-butyl 4-methyl-4-(5-methyl-2-nitrophenylamino)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1.1: tetrahydrofuran; diethyl ether / -15 - 20 °C

2.1: sulfuric acid / 145 h / 20 °C / Cooling with ice-salt bath

2.2: pH 9

3.1: hydrogenchloride; water / 168 h / Heating / reflux

4.1: hydrogen; acetic acid / palladium hydroxide on carbon / methanol / 20 °C / 2585.81 Torr

5.1: potassium carbonate / N,N-dimethyl-formamide / 20 - 110 °C

With hydrogenchloride; sulfuric acid; water; hydrogen; potassium carbonate; acetic acid; palladium hydroxide on carbon; In tetrahydrofuran; methanol; diethyl ether; N,N-dimethyl-formamide;