2-{[(4-methyl-phenyl)-sulfonyl]-hydrazonomethyl}-piperidine-1-carboxylic acid tert-butyl ester

Base Information

• Chemical Name: 2-{[(4-methyl-phenyl)-sulfonyl]-hydrazonomethyl}-piperidine-1-carboxylic acid tert-butyl ester
• CAS No.: 324550-37-0
• Molecular Formula: C₁₈H₂₇N₃O₄S
• Molecular Weight: 381.496
• Mol file: 324550-37-0.mol

Synonyms:2-{[(4-methyl-phenyl)-sulfonyl]-hydrazonomethyl}-piperidine-1-carboxylic acid tert-butyl ester

Chemical Property of 2-{[(4-methyl-phenyl)-sulfonyl]-hydrazonomethyl}-piperidine-1-carboxylic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2-{[(4-methyl-phenyl)-sulfonyl]-hydrazonomethyl}-piperidine-1-carboxylic acid tert-butyl ester

There total 4 articles about 2-{[(4-methyl-phenyl)-sulfonyl]-hydrazonomethyl}-piperidine-1-carboxylic acid tert-butyl ester 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%

tert-butyl 2-formylpiperidine-1-carboxylate (157634-02-1,132910-78-2) + toluene-4-sulfonic acid hydrazide (1576-35-8) → 2-{[(4-methyl-phenyl)-sulfonyl]-hydrazonomethyl}-piperidine-1-carboxylic acid tert-butyl ester (324550-37-0)

Guidance literature:

In ethanol; at 20 ℃; for 0.333333h;

Reference yield:

di-tert-butyl dicarbonate (24424-99-5) → 2-{[(4-methyl-phenyl)-sulfonyl]-hydrazonomethyl}-piperidine-1-carboxylic acid tert-butyl ester (324550-37-0)

Guidance literature:

Multi-step reaction with 3 steps

1: LAH

3: methanol

With lithium aluminium tetrahydride; In methanol; 2: Swern oxidation;

DOI:10.1016/S0040-4039(00)01807-4

Reference yield:

pipecolic Acid (4043-87-2,83680-83-5) → 2-{[(4-methyl-phenyl)-sulfonyl]-hydrazonomethyl}-piperidine-1-carboxylic acid tert-butyl ester (324550-37-0)

Guidance literature:

Multi-step reaction with 3 steps

1: LAH

3: methanol

With lithium aluminium tetrahydride; In methanol; 2: Swern oxidation;

DOI:10.1016/S0040-4039(00)01807-4

upstream raw materials:

tert-butyl 2-formylpiperidine-1-carboxylate

toluene-4-sulfonic acid hydrazide

di-tert-butyl dicarbonate

tert-butyl 2-(hydroxymethyl)piperidine-1-carboxylate

Downstream raw materials:

2-[2-(3-Cyano-phenyl)-2H-tetrazol-5-yl]-piperidine-1-carboxylic acid tert-butyl ester

C₁₈H₂₅N₅O₂

2-[2-(3-chloro-phenyl)-2H-tetrazol-5-yl]-piperidine-1-carboxylic acid tert-butyl ester

C₁₇H₂₂FN₅O₂