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(2S)-2-((2S,4R)-4-(4-((3-(2-(2-(3-aminopropoxy)ethoxy)ethoxy)-propyl)carbamoyl)-1H-1,2,3-triazol-1-yl)-1-(phenylsulfonyl)pyrrolidine-2-carboxamido)-3-(4-((pyrrolidine-1-carbonyl)oxy)phenyl)propanoic acid

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  • Chemical Name:(2S)-2-((2S,4R)-4-(4-((3-(2-(2-(3-aminopropoxy)ethoxy)ethoxy)-propyl)carbamoyl)-1H-1,2,3-triazol-1-yl)-1-(phenylsulfonyl)pyrrolidine-2-carboxamido)-3-(4-((pyrrolidine-1-carbonyl)oxy)phenyl)propanoic acid
  • CAS No.:1541175-36-3
  • Molecular Formula:C38H52N8O11S
  • Molecular Weight:828.944
  • Hs Code.:
(2S)-2-((2S,4R)-4-(4-((3-(2-(2-(3-aminopropoxy)ethoxy)ethoxy)-propyl)carbamoyl)-1H-1,2,3-triazol-1-yl)-1-(phenylsulfonyl)pyrrolidine-2-carboxamido)-3-(4-((pyrrolidine-1-carbonyl)oxy)phenyl)propanoic acid

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Chemical Property of (2S)-2-((2S,4R)-4-(4-((3-(2-(2-(3-aminopropoxy)ethoxy)ethoxy)-propyl)carbamoyl)-1H-1,2,3-triazol-1-yl)-1-(phenylsulfonyl)pyrrolidine-2-carboxamido)-3-(4-((pyrrolidine-1-carbonyl)oxy)phenyl)propanoic acid
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Technology Process of (2S)-2-((2S,4R)-4-(4-((3-(2-(2-(3-aminopropoxy)ethoxy)ethoxy)-propyl)carbamoyl)-1H-1,2,3-triazol-1-yl)-1-(phenylsulfonyl)pyrrolidine-2-carboxamido)-3-(4-((pyrrolidine-1-carbonyl)oxy)phenyl)propanoic acid

There total 15 articles about (2S)-2-((2S,4R)-4-(4-((3-(2-(2-(3-aminopropoxy)ethoxy)ethoxy)-propyl)carbamoyl)-1H-1,2,3-triazol-1-yl)-1-(phenylsulfonyl)pyrrolidine-2-carboxamido)-3-(4-((pyrrolidine-1-carbonyl)oxy)phenyl)propanoic acid 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 7 steps
1: triphenylphosphine; di-isopropyl azodicarboxylate / dichloromethane / 0 - 20 °C / Inert atmosphere
2: toluene; water / 48 h / 80 °C
3: triethylamine / dichloromethane / 2 h / 0 - 20 °C / Inert atmosphere
4: sodium azide / dimethyl sulfoxide / 80 °C
5: sodium L-ascorbate; copper(II) sulfate; tris[(1-benzyl-1H-1,2,3-triazol-4yl)methyl]amine / water; tetrahydrofuran; N,N-dimethyl-formamide / 2 h / 60 °C
6: sodium hydroxide / water; tetrahydrofuran; ethanol / 20 °C
7: palladium 10% on activated carbon; hydrogen / methanol; water / 2 h / 20 °C
With sodium azide; di-isopropyl azodicarboxylate; palladium 10% on activated carbon; hydrogen; copper(II) sulfate; sodium L-ascorbate; triethylamine; triphenylphosphine; sodium hydroxide; tris[(1-benzyl-1H-1,2,3-triazol-4yl)methyl]amine; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide; toluene;
DOI:10.1039/c3ob42332h
Guidance literature:
Multi-step reaction with 6 steps
1.1: potassium carbonate / acetonitrile / 0.75 h / 100 °C / Microwave irradiation
2.1: palladium 10% on activated carbon; hydrogen / methanol / 2 h
3.1: N-ethyl-N,N-diisopropylamine; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate / N,N-dimethyl-formamide / 0.17 h / 0 °C / Inert atmosphere
3.2: 20 °C / Inert atmosphere
4.1: sodium L-ascorbate; copper(II) sulfate; tris[(1-benzyl-1H-1,2,3-triazol-4yl)methyl]amine / water; tetrahydrofuran; N,N-dimethyl-formamide / 2 h / 60 °C
5.1: sodium hydroxide / water; tetrahydrofuran; ethanol / 20 °C
6.1: palladium 10% on activated carbon; hydrogen / methanol; water / 2 h / 20 °C
With palladium 10% on activated carbon; hydrogen; potassium carbonate; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; copper(II) sulfate; sodium L-ascorbate; N-ethyl-N,N-diisopropylamine; sodium hydroxide; tris[(1-benzyl-1H-1,2,3-triazol-4yl)methyl]amine; In tetrahydrofuran; methanol; ethanol; water; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1039/c3ob42332h
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