tert-butyl 4-{[3-(methoxycarbonyl)-2-nitrobenzylidene]amino}-4-methylpiperidine-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-{[3-(methoxycarbonyl)-2-nitrobenzylidene]amino}-4-methylpiperidine-1-carboxylate
CAS No.:1246443-44-6
Molecular Formula:C₂₀H₂₇N₃O₆
Molecular Weight:405.451
Hs Code.:

Synonyms:tert-butyl 4-{[3-(methoxycarbonyl)-2-nitrobenzylidene]amino}-4-methylpiperidine-1-carboxylate

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Chemical Property of tert-butyl 4-{[3-(methoxycarbonyl)-2-nitrobenzylidene]amino}-4-methylpiperidine-1-carboxylate

Chemical Property:

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Technology Process of tert-butyl 4-{[3-(methoxycarbonyl)-2-nitrobenzylidene]amino}-4-methylpiperidine-1-carboxylate

There total 4 articles about tert-butyl 4-{[3-(methoxycarbonyl)-2-nitrobenzylidene]amino}-4-methylpiperidine-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:

: 138229-59-1
3-formyl-2-nitrobenzoic acid methyl ester

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

: 1246443-44-6
tert-butyl 4-{[3-(methoxycarbonyl)-2-nitrobenzylidene]amino}-4-methylpiperidine-1-carboxylate

Guidance literature:: In ethanol; for 24h; Heating / reflux;

Reference yield:

: 132874-06-7
methyl 3-(bromomethyl)-2-nitrobenzoate

: 1246443-44-6
tert-butyl 4-{[3-(methoxycarbonyl)-2-nitrobenzylidene]amino}-4-methylpiperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: 4-methylmorpholine N-oxide / acetonitrile / 1.5 h / 20 °C / Molecular sieve

2: ethanol / 24 h / Heating / reflux

With 4-methylmorpholine N-oxide; In ethanol; acetonitrile;

Reference yield:

: 5437-38-7
3-methyl-2-nitrobenzoic acid

: 1246443-44-6
tert-butyl 4-{[3-(methoxycarbonyl)-2-nitrobenzylidene]amino}-4-methylpiperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: acetyl chloride / 20 h / 0 °C / Heating / reflux

2: N-Bromosuccinimide; dibenzoyl peroxide / tetrachloromethane / 12 h / Heating / reflux

3: 4-methylmorpholine N-oxide / acetonitrile / 1.5 h / 20 °C / Molecular sieve

4: ethanol / 24 h / Heating / reflux

With N-Bromosuccinimide; 4-methylmorpholine N-oxide; acetyl chloride; dibenzoyl peroxide; In tetrachloromethane; ethanol; acetonitrile;