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Nα-Boc-ε-benzyl-D-glutamic acid dipropylamide

Base Information
  • Chemical Name:Nα-Boc-ε-benzyl-D-glutamic acid dipropylamide
  • CAS No.:117997-80-5
  • Molecular Formula:C23H36N2O5
  • Molecular Weight:420.549
  • Hs Code.:
N<sup>α</sup>-Boc-ε-benzyl-D-glutamic acid dipropylamide

Synonyms:Nα-Boc-ε-benzyl-D-glutamic acid dipropylamide

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Chemical Property of Nα-Boc-ε-benzyl-D-glutamic acid dipropylamide
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Technology Process of Nα-Boc-ε-benzyl-D-glutamic acid dipropylamide

There total 4 articles about Nα-Boc-ε-benzyl-D-glutamic acid dipropylamide 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:
With TEA; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; In dichloromethane; at 10 ℃;
DOI:10.1002/(SICI)1099-1344(200001)43:1<77::AID-JLCR292>3.0.CO;2-V
Guidance literature:
Multi-step reaction with 3 steps
1: 20 percent / HI / 20 °C
2: 85 percent / TEA / dimethylformamide; H2O / 20 °C
3: 90 percent / bis(2-oxo-3-oxazolidinyl)phosphinic chloride; TEA / CH2Cl2 / 10 °C
With TEA; hydrogen iodide; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; In dichloromethane; water; N,N-dimethyl-formamide; 1: Esterification / 2: Acylation / 3: amidation;
DOI:10.1002/(SICI)1099-1344(200001)43:1<77::AID-JLCR292>3.0.CO;2-V
Guidance literature:
Multi-step reaction with 2 steps
1: 85 percent / TEA / dimethylformamide; H2O / 20 °C
2: 90 percent / bis(2-oxo-3-oxazolidinyl)phosphinic chloride; TEA / CH2Cl2 / 10 °C
With TEA; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; In dichloromethane; water; N,N-dimethyl-formamide; 1: Acylation / 2: amidation;
DOI:10.1002/(SICI)1099-1344(200001)43:1<77::AID-JLCR292>3.0.CO;2-V
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