(S)-ethyl 1-(2-(3,4,5-trimethoxyphenylamino)pyrimidin-4-yl)piperidine-3-carboxylate

Base Information

Chemical Name:(S)-ethyl 1-(2-(3,4,5-trimethoxyphenylamino)pyrimidin-4-yl)piperidine-3-carboxylate
CAS No.:1347758-04-6
Molecular Formula:C₂₁H₂₈N₄O₅
Molecular Weight:416.477
Hs Code.:

Synonyms:(S)-ethyl 1-(2-(3,4,5-trimethoxyphenylamino)pyrimidin-4-yl)piperidine-3-carboxylate

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Chemical Property of (S)-ethyl 1-(2-(3,4,5-trimethoxyphenylamino)pyrimidin-4-yl)piperidine-3-carboxylate

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Technology Process of (S)-ethyl 1-(2-(3,4,5-trimethoxyphenylamino)pyrimidin-4-yl)piperidine-3-carboxylate

There total 3 articles about (S)-ethyl 1-(2-(3,4,5-trimethoxyphenylamino)pyrimidin-4-yl)piperidine-3-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: 88.0%

: 1347758-03-5
(S)-ethyl 1-(2-chloropyrimidin-4-yl)piperidine-3-carboxylate

: 24313-88-0
3,4,5-Trimethoxyaniline

: 1347758-04-6
(S)-ethyl 1-(2-(3,4,5-trimethoxyphenylamino)pyrimidin-4-yl)piperidine-3-carboxylate

Guidance literature:: In dimethyl sulfoxide; at 90 ℃; for 72h; Inert atmosphere;
DOI:10.1021/jm201565s

Reference yield: 88.0%

: 1347758-04-6
(S)-ethyl 1-(2-(3,4,5-trimethoxyphenylamino)pyrimidin-4-yl)piperidine-3-carboxylate

Guidance literature:

Reference yield:

: 37675-18-6
(S)-(+)-nipecotic acid ethyl ester

: 1347758-04-6
(S)-ethyl 1-(2-(3,4,5-trimethoxyphenylamino)pyrimidin-4-yl)piperidine-3-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / ethanol / 18 h / 0 - 23 °C / Inert atmosphere

2: dimethyl sulfoxide / 72 h / 90 °C / Inert atmosphere

With triethylamine; In ethanol; dimethyl sulfoxide;
DOI:10.1021/jm201565s