(R)-quinuclidin-3-yl ((S)-(3-((4-((2-(1,3-dioxolan-2-yl)ethyl)(benzyl)carbamoyl)benzyl)oxy)phenyl)(phenyl)methyl)carbamate

Base Information

Chemical Name:(R)-quinuclidin-3-yl ((S)-(3-((4-((2-(1,3-dioxolan-2-yl)ethyl)(benzyl)carbamoyl)benzyl)oxy)phenyl)(phenyl)methyl)carbamate
CAS No.:1613464-86-0
Molecular Formula:C₄₁H₄₅N₃O₆
Molecular Weight:675.825
Hs Code.:

Synonyms:(R)-quinuclidin-3-yl ((S)-(3-((4-((2-(1,3-dioxolan-2-yl)ethyl)(benzyl)carbamoyl)benzyl)oxy)phenyl)(phenyl)methyl)carbamate

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Chemical Property of (R)-quinuclidin-3-yl ((S)-(3-((4-((2-(1,3-dioxolan-2-yl)ethyl)(benzyl)carbamoyl)benzyl)oxy)phenyl)(phenyl)methyl)carbamate

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Technology Process of (R)-quinuclidin-3-yl ((S)-(3-((4-((2-(1,3-dioxolan-2-yl)ethyl)(benzyl)carbamoyl)benzyl)oxy)phenyl)(phenyl)methyl)carbamate

There total 8 articles about (R)-quinuclidin-3-yl ((S)-(3-((4-((2-(1,3-dioxolan-2-yl)ethyl)(benzyl)carbamoyl)benzyl)oxy)phenyl)(phenyl)methyl)carbamate 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:

: 1613414-00-8
4-((3-((S)-phenyl(((((R)-quinuclidin-3-yl)oxy)carbonyl)amino)methyl)phenoxy)methyl)benzoic acid

: 134261-49-7
N-benzyl-2-(1,3-dioxolan-2-yl)ethanamine

: 1613464-86-0
(R)-quinuclidin-3-yl ((S)-(3-((4-((2-(1,3-dioxolan-2-yl)ethyl)(benzyl)carbamoyl)benzyl)oxy)phenyl)(phenyl)methyl)carbamate

Guidance literature:: 4-((3-((S)-phenyl(((((R)-quinuclidin-3-yl)oxy)carbonyl)amino)methyl)phenoxy)methyl)benzoic acid; With 2-hydroxy-pyridine N-oxide; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In N,N-dimethyl-formamide; at 20 ℃; for 0.166667h;

N-benzyl-2-(1,3-dioxolan-2-yl)ethanamine; In N,N-dimethyl-formamide; at 20 - 40 ℃; for 52h;

Reference yield:

: 1613413-98-1
(S)-methyl 4-((3-(amino(phenyl)methyl)phenoxy)methyl)benzoate hydrochloride

: 1613464-86-0
(R)-quinuclidin-3-yl ((S)-(3-((4-((2-(1,3-dioxolan-2-yl)ethyl)(benzyl)carbamoyl)benzyl)oxy)phenyl)(phenyl)methyl)carbamate

Guidance literature:: Multi-step reaction with 3 steps

1.1: pyridine / 17 h / 0 - 20 °C

2.1: water; lithium hydroxide / tetrahydrofuran / 16 h / 20 °C

3.1: 2-hydroxy-pyridine N-oxide; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / N,N-dimethyl-formamide / 0.17 h / 20 °C

3.2: 52 h / 20 - 40 °C

With pyridine; 2-hydroxy-pyridine N-oxide; water; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; lithium hydroxide; In tetrahydrofuran; N,N-dimethyl-formamide;

Reference yield:

: 1416070-91-1
(S)-tert-butyl ((3-hydroxyphenyl)(phenyl)methyl)carbamate

: 1613464-86-0
(R)-quinuclidin-3-yl ((S)-(3-((4-((2-(1,3-dioxolan-2-yl)ethyl)(benzyl)carbamoyl)benzyl)oxy)phenyl)(phenyl)methyl)carbamate

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium carbonate / acetonitrile / 16 h / 20 °C

2.1: hydrogenchloride / methanol; 1,4-dioxane / 16 h / 20 °C

3.1: pyridine / 17 h / 0 - 20 °C

4.1: water; lithium hydroxide / tetrahydrofuran / 16 h / 20 °C

5.1: 2-hydroxy-pyridine N-oxide; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / N,N-dimethyl-formamide / 0.17 h / 20 °C

5.2: 52 h / 20 - 40 °C

With pyridine; hydrogenchloride; 2-hydroxy-pyridine N-oxide; water; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; lithium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; N,N-dimethyl-formamide; acetonitrile;