Tert-butyl 4-{4-[5-(5-tert-butyl-3-methanesulphonyl-2-methoxy-phenylcarbamoyl)-2-methyl-phenoxy]-pyridin-2-ylmethyl}-piperidine-1-carboxylate

Base Information

Chemical Name:Tert-butyl 4-{4-[5-(5-tert-butyl-3-methanesulphonyl-2-methoxy-phenylcarbamoyl)-2-methyl-phenoxy]-pyridin-2-ylmethyl}-piperidine-1-carboxylate
CAS No.:1215031-80-3
Molecular Formula:C₃₆H₄₇N₃O₇S
Molecular Weight:665.851
Hs Code.:

Tert-butyl 4-{4-[5-(5-tert-butyl-3-methanesulphonyl-2-methoxy-phenylcarbamoyl)-2-methyl-phenoxy]-pyridin-2-ylmethyl}-piperidine-1-carboxylate

Synonyms:Tert-butyl 4-{4-[5-(5-tert-butyl-3-methanesulphonyl-2-methoxy-phenylcarbamoyl)-2-methyl-phenoxy]-pyridin-2-ylmethyl}-piperidine-1-carboxylate

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Chemical Property of Tert-butyl 4-{4-[5-(5-tert-butyl-3-methanesulphonyl-2-methoxy-phenylcarbamoyl)-2-methyl-phenoxy]-pyridin-2-ylmethyl}-piperidine-1-carboxylate

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Technology Process of Tert-butyl 4-{4-[5-(5-tert-butyl-3-methanesulphonyl-2-methoxy-phenylcarbamoyl)-2-methyl-phenoxy]-pyridin-2-ylmethyl}-piperidine-1-carboxylate

There total 3 articles about Tert-butyl 4-{4-[5-(5-tert-butyl-3-methanesulphonyl-2-methoxy-phenylcarbamoyl)-2-methyl-phenoxy]-pyridin-2-ylmethyl}-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: 54.0%

: 1215031-53-0
5-(tert-butyl)-2-methoxy-3-(methylsulfonyl)aniline

: 1215031-04-1
tert-butyl 4-[4-(5-carboxy-2-methyl-phenoxy)-pyridin-2-ylmethyl]-piperidine-1-carboxylate

: 1215031-80-3
Tert-butyl 4-{4-[5-(5-tert-butyl-3-methanesulphonyl-2-methoxy-phenylcarbamoyl)-2-methyl-phenoxy]-pyridin-2-ylmethyl}-piperidine-1-carboxylate

Guidance literature:: tert-butyl 4-[4-(5-carboxy-2-methyl-phenoxy)-pyridin-2-ylmethyl]-piperidine-1-carboxylate; With oxalyl dichloride; In acetonitrile; at 20 ℃; for 2h;

5-(tert-butyl)-2-methoxy-3-(methylsulfonyl)aniline; With triethylamine; In 1,2-dichloro-ethane; at 20 ℃;

Reference yield:

: 1215031-63-2
5-tert-butyl-1-methanesulphonyl-2-methoxy-3-nitro-benzene

: 1215031-80-3
Tert-butyl 4-{4-[5-(5-tert-butyl-3-methanesulphonyl-2-methoxy-phenylcarbamoyl)-2-methyl-phenoxy]-pyridin-2-ylmethyl}-piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1.1: hydrogen / palladium 10% on activated carbon / methanol / 6 h / 20 °C / 2585.81 Torr

2.1: oxalyl dichloride / acetonitrile / 2 h / 20 °C

2.2: 20 °C

With oxalyl dichloride; hydrogen; palladium 10% on activated carbon; In methanol; acetonitrile;

Reference yield:

: 1215032-00-0
(5-(tert-butyl)-2-methoxy-3-nitrophenyl)(methyl)sulfane

: 1215031-80-3
Tert-butyl 4-{4-[5-(5-tert-butyl-3-methanesulphonyl-2-methoxy-phenylcarbamoyl)-2-methyl-phenoxy]-pyridin-2-ylmethyl}-piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 6 h / 20 °C / Cooling with ice

2.1: hydrogen / palladium 10% on activated carbon / methanol / 6 h / 20 °C / 2585.81 Torr

3.1: oxalyl dichloride / acetonitrile / 2 h / 20 °C

3.2: 20 °C

With oxalyl dichloride; hydrogen; 3-chloro-benzenecarboperoxoic acid; palladium 10% on activated carbon; In methanol; dichloromethane; acetonitrile;