[5-(1-methylamino-ethyl)-furan-2-yl]-[(2S,4R)-4-phenyl-2-((R)-3-phenyl-pyrrolidine-1-carbonyl)-pyrrolidin-1-yl]-methanone

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Chemical Name:[5-(1-methylamino-ethyl)-furan-2-yl]-[(2S,4R)-4-phenyl-2-((R)-3-phenyl-pyrrolidine-1-carbonyl)-pyrrolidin-1-yl]-methanone
CAS No.:1201986-92-6
Molecular Formula:C₂₉H₃₃N₃O₃
Molecular Weight:471.599
Hs Code.:

Synonyms:[5-(1-methylamino-ethyl)-furan-2-yl]-[(2S,4R)-4-phenyl-2-((R)-3-phenyl-pyrrolidine-1-carbonyl)-pyrrolidin-1-yl]-methanone

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Chemical Property of [5-(1-methylamino-ethyl)-furan-2-yl]-[(2S,4R)-4-phenyl-2-((R)-3-phenyl-pyrrolidine-1-carbonyl)-pyrrolidin-1-yl]-methanone

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Technology Process of [5-(1-methylamino-ethyl)-furan-2-yl]-[(2S,4R)-4-phenyl-2-((R)-3-phenyl-pyrrolidine-1-carbonyl)-pyrrolidin-1-yl]-methanone

There total 7 articles about [5-(1-methylamino-ethyl)-furan-2-yl]-[(2S,4R)-4-phenyl-2-((R)-3-phenyl-pyrrolidine-1-carbonyl)-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: 55.0%

: 1201986-87-9
methyl-(1-{5-[(2S,4R)-4-phenyl-2-((R)-3-phenyl-pyrrolidine-1-carbonyl)-pyrrolidine-1-carbonyl]-furan-2-yl}-ethyl)-carbamic acid tert-butyl ester

: 1201986-92-6
[5-(1-methylamino-ethyl)-furan-2-yl]-[(2S,4R)-4-phenyl-2-((R)-3-phenyl-pyrrolidine-1-carbonyl)-pyrrolidin-1-yl]-methanone

Guidance literature:: methyl-(1-{5-[(2S,4R)-4-phenyl-2-((R)-3-phenyl-pyrrolidine-1-carbonyl)-pyrrolidine-1-carbonyl]-furan-2-yl}-ethyl)-carbamic acid tert-butyl ester; With hydrogenchloride; water; In 1,4-dioxane; at 18 - 25 ℃; for 2h;

In tetrahydrofuran; at 18 - 25 ℃; for 2h;

Reference yield:

: 614-99-3
Ethyl 2-furoate

: 1201986-92-6
[5-(1-methylamino-ethyl)-furan-2-yl]-[(2S,4R)-4-phenyl-2-((R)-3-phenyl-pyrrolidine-1-carbonyl)-pyrrolidin-1-yl]-methanone

Guidance literature:: Multi-step reaction with 4 steps

1.1: boron trifluoride-tetrahydrofuran complex / 0 - 25 °C

2.1: tetrahydrofuran / 16 h / 18 - 25 °C

2.2: 16 h / 18 - 25 °C

3.1: N-ethyl-N,N-diisopropylamine; HATU / dichloromethane; N,N-dimethyl-formamide / 16 h / 18 - 25 °C

4.1: hydrogenchloride; water / 1,4-dioxane / 2 h / 18 - 25 °C

4.2: Si-carbonate / 2 h / 18 - 25 °C

With hydrogenchloride; water; N-ethyl-N,N-diisopropylamine; HATU; boron trifluoride-tetrahydrofuran complex; In tetrahydrofuran; 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide; 1.1: Friedel Crafts Acylation;

Reference yield:

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

: 1201986-92-6
[5-(1-methylamino-ethyl)-furan-2-yl]-[(2S,4R)-4-phenyl-2-((R)-3-phenyl-pyrrolidine-1-carbonyl)-pyrrolidin-1-yl]-methanone

Guidance literature:: Multi-step reaction with 3 steps

1.1: hydrogenchloride; water / 1,4-dioxane / 1 h / 18 - 25 °C

2.1: N-ethyl-N,N-diisopropylamine; HATU / dichloromethane; N,N-dimethyl-formamide / 16 h / 18 - 25 °C

3.1: hydrogenchloride; water / 1,4-dioxane / 2 h / 18 - 25 °C

3.2: Si-carbonate / 2 h / 18 - 25 °C

With hydrogenchloride; water; N-ethyl-N,N-diisopropylamine; HATU; In 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide;