tert-butyl 4-[3-(N,,N-dimethylcarbamoyloxy)phenylcarbamoyl]-4-methylpiperidine-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-[3-(N,,N-dimethylcarbamoyloxy)phenylcarbamoyl]-4-methylpiperidine-1-carboxylate
CAS No.:1192189-46-0
Molecular Formula:C₂₁H₃₁N₃O₅
Molecular Weight:405.494
Hs Code.:

Synonyms:tert-butyl 4-[3-(N,,N-dimethylcarbamoyloxy)phenylcarbamoyl]-4-methylpiperidine-1-carboxylate

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Chemical Property of tert-butyl 4-[3-(N,,N-dimethylcarbamoyloxy)phenylcarbamoyl]-4-methylpiperidine-1-carboxylate

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Technology Process of tert-butyl 4-[3-(N,,N-dimethylcarbamoyloxy)phenylcarbamoyl]-4-methylpiperidine-1-carboxylate

There total 1 articles about tert-butyl 4-[3-(N,,N-dimethylcarbamoyloxy)phenylcarbamoyl]-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: 50.0%

: 19962-04-0
Dimethylcarbaminsaeure-3-aminophenylester

: 189321-63-9
1-(tert-butoxycarbonyl)-4-methylpiperidine-4-carboxylic acid

: 1192189-46-0
tert-butyl 4-[3-(N,,N-dimethylcarbamoyloxy)phenylcarbamoyl]-4-methylpiperidine-1-carboxylate

Guidance literature:: 1-(tert-butoxycarbonyl)-4-methylpiperidine-4-carboxylic acid; With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In 1,2-dichloro-ethane; for 0.75h;

Dimethylcarbaminsaeure-3-aminophenylester; In 1,2-dichloro-ethane; at 85 ℃; for 18h;

Reference yield:

: 1192189-46-0
tert-butyl 4-[3-(N,,N-dimethylcarbamoyloxy)phenylcarbamoyl]-4-methylpiperidine-1-carboxylate

: 1192189-45-9
3-(4-methyl-1-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidine-4-carboxamido)phenyl N,N-dimethylcarbamate

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride; methanol / 1,4-dioxane / 3 h / 40 °C / Inert atmosphere

2: N-ethyl-N,N-diisopropylamine / isopropyl alcohol / 18 h / 100 °C / Inert atmosphere; High pressure

With hydrogenchloride; methanol; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; isopropyl alcohol;
DOI:10.1021/ml500367g