tert-butyl 4-(2-pyrrolidin-1-ylethoxymethyl)piperidine-1-carboxylate

Base Information

• Chemical Name: tert-butyl 4-(2-pyrrolidin-1-ylethoxymethyl)piperidine-1-carboxylate
• CAS No.: 1437774-69-0
• Molecular Formula: C₁₇H₃₂N₂O₃
• Molecular Weight: 312.453
• Mol file: 1437774-69-0.mol

Synonyms:tert-butyl 4-(2-pyrrolidin-1-ylethoxymethyl)piperidine-1-carboxylate

Chemical Property of tert-butyl 4-(2-pyrrolidin-1-ylethoxymethyl)piperidine-1-carboxylate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of tert-butyl 4-(2-pyrrolidin-1-ylethoxymethyl)piperidine-1-carboxylate

There total 2 articles about tert-butyl 4-(2-pyrrolidin-1-ylethoxymethyl)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: 76.0%

1-(2-chloroethyl)pyrrolidine hydrochloride (7250-67-1) + tert-butyl 4-(hydroxymethyl)piperidin-1-carboxylate (123855-51-6) → tert-butyl 4-(2-pyrrolidin-1-ylethoxymethyl)piperidine-1-carboxylate (1437774-69-0)

Guidance literature:

With tetrabutylammomium bromide; sodium hydroxide; In water; toluene; at 80 ℃; for 16h;

Reference yield:

N-(2-chloroethyl)-pyrrolidine (5050-41-9) + tert-butyl 4-(hydroxymethyl)piperidin-1-carboxylate (123855-51-6) → tert-butyl 4-(2-pyrrolidin-1-ylethoxymethyl)piperidine-1-carboxylate (1437774-69-0)

Guidance literature:

With tetrabutylammomium bromide; In water; toluene; at 90 ℃;

Reference yield:

tert-butyl 4-(2-pyrrolidin-1-ylethoxymethyl)piperidine-1-carboxylate (1437774-69-0) → 1-[4-phenyl-3-[4-(2-pyrrolidin-1-ylethoxymethyl)-1-piperidyl]thieno[2,3-c]pyrazol-1-yl]ethanone (1436612-18-8)

Guidance literature:

Multi-step reaction with 5 steps

1: trifluoroacetic acid / dichloromethane / 2 h / 20 °C

2: 1,4-diaza-bicyclo[2.2.2]octane / tetrahydrofuran / 20 °C

3: copper(l) iodide; potassium carbonate / 1-methyl-pyrrolidin-2-one / 1 h / 180 °C / Microwave irradiation

4: potassium hydroxide / methanol / 0.5 h / Reflux

5: triethylamine / dichloromethane / 1 h / 0 - 20 °C

With 1,4-diaza-bicyclo[2.2.2]octane; copper(l) iodide; potassium carbonate; triethylamine; trifluoroacetic acid; potassium hydroxide; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; methanol; dichloromethane;

upstream raw materials:

1-(2-chloroethyl)pyrrolidine hydrochloride

tert-butyl 4-(hydroxymethyl)piperidin-1-carboxylate

N-(2-chloroethyl)-pyrrolidine

Downstream raw materials:

1-[4-phenyl-3-[4-(2-pyrrolidin-1-ylethoxymethyl)-1-piperidyl]thieno[2,3-c]pyrazol-1-yl]ethanone

4-(2-pyrrolidin-1-ylethoxymethyl)piperidine

4-phenyl-1-(p-tolylsulfonyl)-3-[4-(2-pyrrolidin-1-ylethoxymethyl)-1-piperidyl]thieno[2,3-c]pyrazole

4-phenyl-3-[4-(2-pyrrolidin-1-ylethoxymethyl)-1-piperidyl]-1H-thieno[2,3-c]pyrazole