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N-[4-({(2S,5R)-5-[(R)-hydroxy(pyridin-3-yl)methyl]pyrrolidin-2-yl}methyl)phenyl]-2-(2-oxopyrrolidin-1-yl)acetamide trifluoroacetamide

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  • Chemical Name:N-[4-({(2S,5R)-5-[(R)-hydroxy(pyridin-3-yl)methyl]pyrrolidin-2-yl}methyl)phenyl]-2-(2-oxopyrrolidin-1-yl)acetamide trifluoroacetamide
  • CAS No.:1190609-33-6
  • Molecular Formula:C2HF3O2*C23H28N4O3
  • Molecular Weight:522.524
  • Hs Code.:
N-[4-({(2S,5R)-5-[(R)-hydroxy(pyridin-3-yl)methyl]pyrrolidin-2-yl}methyl)phenyl]-2-(2-oxopyrrolidin-1-yl)acetamide trifluoroacetamide

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Chemical Property of N-[4-({(2S,5R)-5-[(R)-hydroxy(pyridin-3-yl)methyl]pyrrolidin-2-yl}methyl)phenyl]-2-(2-oxopyrrolidin-1-yl)acetamide trifluoroacetamide
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Technology Process of N-[4-({(2S,5R)-5-[(R)-hydroxy(pyridin-3-yl)methyl]pyrrolidin-2-yl}methyl)phenyl]-2-(2-oxopyrrolidin-1-yl)acetamide trifluoroacetamide

There total 13 articles about N-[4-({(2S,5R)-5-[(R)-hydroxy(pyridin-3-yl)methyl]pyrrolidin-2-yl}methyl)phenyl]-2-(2-oxopyrrolidin-1-yl)acetamide trifluoroacetamide 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:
Guidance literature:
Multi-step reaction with 14 steps
1.1: chloro-trimethyl-silane; triethylamine; magnesium chloride / ethyl acetate / 72 h / 20 °C
2.1: trifluoroacetic acid / methanol / 5 h / 20 °C
3.1: 2,6-dimethylpyridine / dichloromethane / 0 - 3 °C
4.1: water; dihydrogen peroxide; sodium hydroxide / tetrahydrofuran / 0 - 5 °C
4.2: 15 °C
4.3: 0 °C / pH 3
5.1: diphenyl phosphoryl azide; triethylamine / toluene / 6 h / 20 °C
5.2: 16 h / 100 °C
6.1: triethylamine / copper(l) iodide; tetrakis(triphenylphosphine) palladium(0) / acetonitrile / 15 h / 20 °C
7.1: pyrrolidine / N,N-dimethyl-formamide / 5 h / 80 °C
7.2: 3 h / 20 °C
8.1: trifluoroacetic acid / dichloromethane / 2 h / 20 °C
9.1: methanol; sodium cyanoborohydride / 0 °C
10.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 4 h / 20 °C
11.1: hydrogen; potassium acetate / palladium 10% on activated carbon / ethanol / 8 h / 2585.81 Torr
12.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 7 h
13.1: 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 24 h / 20 °C
13.2: HPLC
14.1: hydrogenchloride / 1,3-dioxane; isopropyl alcohol / 1 h
14.2: HPLC
With pyrrolidine; 2,6-dimethylpyridine; hydrogenchloride; methanol; chloro-trimethyl-silane; 1-hydroxy-7-aza-benzotriazole; diphenyl phosphoryl azide; tetrabutyl ammonium fluoride; water; hydrogen; dihydrogen peroxide; potassium acetate; sodium cyanoborohydride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; sodium hydroxide; magnesium chloride; copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); palladium 10% on activated carbon; In tetrahydrofuran; 1,3-dioxane; methanol; ethanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide; isopropyl alcohol; toluene; acetonitrile;
Guidance literature:
Multi-step reaction with 10 steps
1.1: diphenyl phosphoryl azide; triethylamine / toluene / 6 h / 20 °C
1.2: 16 h / 100 °C
2.1: triethylamine / copper(l) iodide; tetrakis(triphenylphosphine) palladium(0) / acetonitrile / 15 h / 20 °C
3.1: pyrrolidine / N,N-dimethyl-formamide / 5 h / 80 °C
3.2: 3 h / 20 °C
4.1: trifluoroacetic acid / dichloromethane / 2 h / 20 °C
5.1: methanol; sodium cyanoborohydride / 0 °C
6.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 4 h / 20 °C
7.1: hydrogen; potassium acetate / palladium 10% on activated carbon / ethanol / 8 h / 2585.81 Torr
8.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 7 h
9.1: 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 24 h / 20 °C
9.2: HPLC
10.1: hydrogenchloride / 1,3-dioxane; isopropyl alcohol / 1 h
10.2: HPLC
With pyrrolidine; hydrogenchloride; methanol; 1-hydroxy-7-aza-benzotriazole; diphenyl phosphoryl azide; tetrabutyl ammonium fluoride; hydrogen; potassium acetate; sodium cyanoborohydride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); palladium 10% on activated carbon; In tetrahydrofuran; 1,3-dioxane; ethanol; dichloromethane; N,N-dimethyl-formamide; isopropyl alcohol; toluene; acetonitrile;
Guidance literature:
Multi-step reaction with 5 steps
1.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 4 h / 20 °C
2.1: hydrogen; potassium acetate / palladium 10% on activated carbon / ethanol / 8 h / 2585.81 Torr
3.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 7 h
4.1: 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 24 h / 20 °C
4.2: HPLC
5.1: hydrogenchloride / 1,3-dioxane; isopropyl alcohol / 1 h
5.2: HPLC
With hydrogenchloride; 1-hydroxy-7-aza-benzotriazole; tetrabutyl ammonium fluoride; hydrogen; potassium acetate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; palladium 10% on activated carbon; In tetrahydrofuran; 1,3-dioxane; ethanol; dichloromethane; N,N-dimethyl-formamide; isopropyl alcohol;
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