{[[2-(3,4-Dichloro-phenyl)-ethyl]-(2-pyrrolidin-1-yl-ethyl)-carbamoyl]-methyl}-carbamic acid tert-butyl ester

Base Information

• Chemical Name: {[[2-(3,4-Dichloro-phenyl)-ethyl]-(2-pyrrolidin-1-yl-ethyl)-carbamoyl]-methyl}-carbamic acid tert-butyl ester
• CAS No.: 153906-03-7
• Molecular Formula: C₂₁H₃₁Cl₂N₃O₃
• Molecular Weight: 444.401
• Mol file: 153906-03-7.mol

Synonyms:{[[2-(3,4-Dichloro-phenyl)-ethyl]-(2-pyrrolidin-1-yl-ethyl)-carbamoyl]-methyl}-carbamic acid tert-butyl ester

Chemical Property of {[[2-(3,4-Dichloro-phenyl)-ethyl]-(2-pyrrolidin-1-yl-ethyl)-carbamoyl]-methyl}-carbamic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of {[[2-(3,4-Dichloro-phenyl)-ethyl]-(2-pyrrolidin-1-yl-ethyl)-carbamoyl]-methyl}-carbamic acid tert-butyl ester

There total 1 articles about {[[2-(3,4-Dichloro-phenyl)-ethyl]-(2-pyrrolidin-1-yl-ethyl)-carbamoyl]-methyl}-carbamic 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:

BOC-glycine (4530-20-5) + BD 1060 (138356-10-2) → {[[2-(3,4-Dichloro-phenyl)-ethyl]-(2-pyrrolidin-1-yl-ethyl)-carbamoyl]-methyl}-carbamic acid tert-butyl ester (153906-03-7)

Guidance literature:

With dicyclohexyl-carbodiimide; In dichloromethane; Ambient temperature;

DOI:10.1021/jm00028a016

Reference yield: 66.0%

{[[2-(3,4-Dichloro-phenyl)-ethyl]-(2-pyrrolidin-1-yl-ethyl)-carbamoyl]-methyl}-carbamic acid tert-butyl ester (153906-03-7) → N-<2-(3,4-dichlorophenyl)ethyl>-N-glycyl-2-(1-pyrrolidinyl)ethylamine

Guidance literature:

With trifluoroacetic acid; In chloroform; for 2h; Ambient temperature;

DOI:10.1021/jm00028a016

Reference yield:

{[[2-(3,4-Dichloro-phenyl)-ethyl]-(2-pyrrolidin-1-yl-ethyl)-carbamoyl]-methyl}-carbamic acid tert-butyl ester (153906-03-7) → N1-[2-(3,4-Dichloro-phenyl)-ethyl]-N1-(2-pyrrolidin-1-yl-ethyl)-ethane-1,2-diamine

Guidance literature:

Multi-step reaction with 2 steps

1: 66 percent / CF₃CO₂H / CHCl₃ / 2 h / Ambient temperature

2: AlH₃ / tetrahydrofuran / Ambient temperature

With aluminium hydride; trifluoroacetic acid; In tetrahydrofuran; chloroform;

DOI:10.1021/jm00028a016

upstream raw materials:

BOC-glycine

BD 1060