2-[(3S)-1-cyclopropylcarbonyl-3-pyrrolidinyl]-N-methyl-N-[4-(2-naphthalenyl)phenyl]acetamide

Base Information

Chemical Name:2-[(3S)-1-cyclopropylcarbonyl-3-pyrrolidinyl]-N-methyl-N-[4-(2-naphthalenyl)phenyl]acetamide
CAS No.:1426095-52-4
Molecular Formula:C₂₇H₂₈N₂O₂
Molecular Weight:412.532
Hs Code.:

Synonyms:2-[(3S)-1-cyclopropylcarbonyl-3-pyrrolidinyl]-N-methyl-N-[4-(2-naphthalenyl)phenyl]acetamide

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Chemical Property of 2-[(3S)-1-cyclopropylcarbonyl-3-pyrrolidinyl]-N-methyl-N-[4-(2-naphthalenyl)phenyl]acetamide

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Technology Process of 2-[(3S)-1-cyclopropylcarbonyl-3-pyrrolidinyl]-N-methyl-N-[4-(2-naphthalenyl)phenyl]acetamide

There total 5 articles about 2-[(3S)-1-cyclopropylcarbonyl-3-pyrrolidinyl]-N-methyl-N-[4-(2-naphthalenyl)phenyl]acetamide 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:

: 1426096-33-4
N-(4-bromophenyl)-2-[(3S)-1-cyclopropylcarbonyl-3-pyrrolidinyl]-N-methylacetamide

: 32316-92-0
naphthalene-2-boronic acid

: 1426095-52-4
2-[(3S)-1-cyclopropylcarbonyl-3-pyrrolidinyl]-N-methyl-N-[4-(2-naphthalenyl)phenyl]acetamide

Guidance literature:: With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium carbonate; In 1,4-dioxane; water; at 95 ℃; for 18h;

Reference yield:

: 204688-61-9
2‐[(3S)‐1‐[(tert‐butoxy)carbonyl]pyrrolidin‐3‐yl]acetic acid

: 1426095-52-4
2-[(3S)-1-cyclopropylcarbonyl-3-pyrrolidinyl]-N-methyl-N-[4-(2-naphthalenyl)phenyl]acetamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: 4-methyl-morpholine; chloroformic acid ethyl ester / tetrahydrofuran / 0.17 h / 0 °C

1.2: 18 h / 20 °C

2.1: trifluoroacetic acid / dichloromethane / 20 h / 20 °C

2.2: 0.5 h / 0 °C

3.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.25 h / 20 °C

3.2: 0.5 h

4.1: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium carbonate / 1,4-dioxane; water / 18 h / 95 °C

With 4-methyl-morpholine; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; chloroformic acid ethyl ester; sodium hydride; potassium carbonate; trifluoroacetic acid; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 106-40-1
4-bromo-aniline

: 1426095-52-4
2-[(3S)-1-cyclopropylcarbonyl-3-pyrrolidinyl]-N-methyl-N-[4-(2-naphthalenyl)phenyl]acetamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: 4-methyl-morpholine; chloroformic acid ethyl ester / tetrahydrofuran / 0.17 h / 0 °C

1.2: 18 h / 20 °C

2.1: trifluoroacetic acid / dichloromethane / 20 h / 20 °C

2.2: 0.5 h / 0 °C

3.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.25 h / 20 °C

3.2: 0.5 h

4.1: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium carbonate / 1,4-dioxane; water / 18 h / 95 °C

With 4-methyl-morpholine; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; chloroformic acid ethyl ester; sodium hydride; potassium carbonate; trifluoroacetic acid; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water; N,N-dimethyl-formamide; mineral oil;