(5-(1-aminoethyl)furan-2-yl)((2S,4R)-4-phenyl-2-(((R)-3-phenylpyrrolidin-1-yl)methyl)pyrrolidin-1-yl)methanone

Base Information

Chemical Name:(5-(1-aminoethyl)furan-2-yl)((2S,4R)-4-phenyl-2-(((R)-3-phenylpyrrolidin-1-yl)methyl)pyrrolidin-1-yl)methanone
CAS No.:1201986-93-7
Molecular Formula:C₂₈H₃₃N₃O₂
Molecular Weight:443.589
Hs Code.:

Synonyms:(5-(1-aminoethyl)furan-2-yl)((2S,4R)-4-phenyl-2-(((R)-3-phenylpyrrolidin-1-yl)methyl)pyrrolidin-1-yl)methanone

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Chemical Property of (5-(1-aminoethyl)furan-2-yl)((2S,4R)-4-phenyl-2-(((R)-3-phenylpyrrolidin-1-yl)methyl)pyrrolidin-1-yl)methanone

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Technology Process of (5-(1-aminoethyl)furan-2-yl)((2S,4R)-4-phenyl-2-(((R)-3-phenylpyrrolidin-1-yl)methyl)pyrrolidin-1-yl)methanone

There total 5 articles about (5-(1-aminoethyl)furan-2-yl)((2S,4R)-4-phenyl-2-(((R)-3-phenylpyrrolidin-1-yl)methyl)pyrrolidin-1-yl)methanone 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:

: 1201986-89-1
2-nitro-N-(1-(5-((2S,4R)-4-phenyl-2-(((R)-3-phenyprrolidin-1-yl)methyl)pyrrolidine-1-carbonyl)furan-2-yl)ethyl)benzenesulfonamide

: 1201986-93-7
(5-(1-aminoethyl)furan-2-yl)((2S,4R)-4-phenyl-2-(((R)-3-phenylpyrrolidin-1-yl)methyl)pyrrolidin-1-yl)methanone

Guidance literature:: With 4-Methoxybenzenethiol; caesium carbonate; In tetrahydrofuran; at 18 - 25 ℃; for 16h;

Reference yield:

: 1201986-77-7
(2S,4R)-tert-butyl-4-phenyl-2-((R)-3-phenylpyrrolidine-1-carbonyl)pyrrolidine-1-carboxylate

: 1201986-93-7
(5-(1-aminoethyl)furan-2-yl)((2S,4R)-4-phenyl-2-(((R)-3-phenylpyrrolidin-1-yl)methyl)pyrrolidin-1-yl)methanone

Guidance literature:: Multi-step reaction with 3 steps

1.1: dimethylsulfide borane complex / 1,4-dioxane / 16 h / 80 °C / Inert atmosphere

1.2: 18 - 25 °C

2.1: benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 16 h / 18 - 25 °C

3.1: 4-Methoxybenzenethiol; caesium carbonate / tetrahydrofuran / 16 h / 18 - 25 °C

With 4-Methoxybenzenethiol; dimethylsulfide borane complex; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; caesium carbonate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; 1,4-dioxane; N,N-dimethyl-formamide;

Reference yield:

: 1201986-73-3
(2S,4R)-4-phenyl-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-(4-oxo-4H-benzo[d][1,2,3]triazin-3-yl) ester

: 1201986-93-7
(5-(1-aminoethyl)furan-2-yl)((2S,4R)-4-phenyl-2-(((R)-3-phenylpyrrolidin-1-yl)methyl)pyrrolidin-1-yl)methanone

Guidance literature:: Multi-step reaction with 4 steps

1.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 16 h / 18 - 25 °C

2.1: dimethylsulfide borane complex / 1,4-dioxane / 16 h / 80 °C / Inert atmosphere

2.2: 18 - 25 °C

3.1: benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 16 h / 18 - 25 °C

4.1: 4-Methoxybenzenethiol; caesium carbonate / tetrahydrofuran / 16 h / 18 - 25 °C

With 4-Methoxybenzenethiol; dimethylsulfide borane complex; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; caesium carbonate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; 1,4-dioxane; N,N-dimethyl-formamide; acetonitrile;