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3-{Nα-[6-({N-[2-(benzyloxycarbonylamino)ethyl]-N-(benzyloxycarbonyl)amino}methyl)-2-pyridylcarbonyl]-L-histidinylamino}-N-t-butylpropionamide

Base Information Edit
  • Chemical Name:3-{Nα-[6-({N-[2-(benzyloxycarbonylamino)ethyl]-N-(benzyloxycarbonyl)amino}methyl)-2-pyridylcarbonyl]-L-histidinylamino}-N-t-butylpropionamide
  • CAS No.:209467-31-2
  • Molecular Formula:C38H46N8O7
  • Molecular Weight:726.833
  • Hs Code.:
  • Mol file:209467-31-2.mol
3-{N<sup>α</sup>-[6-({N-[2-(benzyloxycarbonylamino)ethyl]-N-(benzyloxycarbonyl)amino}methyl)-2-pyridylcarbonyl]-L-histidinylamino}-N-t-butylpropionamide

Synonyms:

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 3-{Nα-[6-({N-[2-(benzyloxycarbonylamino)ethyl]-N-(benzyloxycarbonyl)amino}methyl)-2-pyridylcarbonyl]-L-histidinylamino}-N-t-butylpropionamide Edit
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Technology Process of 3-{Nα-[6-({N-[2-(benzyloxycarbonylamino)ethyl]-N-(benzyloxycarbonyl)amino}methyl)-2-pyridylcarbonyl]-L-histidinylamino}-N-t-butylpropionamide

There total 7 articles about 3-{Nα-[6-({N-[2-(benzyloxycarbonylamino)ethyl]-N-(benzyloxycarbonyl)amino}methyl)-2-pyridylcarbonyl]-L-histidinylamino}-N-t-butylpropionamide 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: molecular sieve (4 Angstroem) / acetonitrile / 20 °C
2: NaBH4 / methanol / 2 h / 20 °C
3: 4.86 g / aq. NaOH / CH2Cl2 / 3 h / 20 °C
4: aq. LiOH / tetrahydrofuran / 2 h / 0 °C
5: 615 mg / diphenylphosphoryl azide; Et3N / dimethylformamide / 75 h / 0 - 20 °C
6: aq. LiOH / tetrahydrofuran / 2 h / 0 °C
7: 602 mg / diphenylphosphoryl azide; Et3N / dimethylformamide / 51 h / 0 - 20 °C
With lithium hydroxide; sodium hydroxide; sodium tetrahydroborate; 4 A molecular sieve; diphenylphosphoranyl azide; triethylamine; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile; 1: Condensation / 2: Reduction / 3: Acylation / 4: Hydrolysis / 5: Condensation / 6: Hydrolysis / 7: Condensation;
DOI:10.1246/bcsj.71.1159
Guidance literature:
Multi-step reaction with 3 steps
1: 615 mg / diphenylphosphoryl azide; Et3N / dimethylformamide / 75 h / 0 - 20 °C
2: aq. LiOH / tetrahydrofuran / 2 h / 0 °C
3: 602 mg / diphenylphosphoryl azide; Et3N / dimethylformamide / 51 h / 0 - 20 °C
With lithium hydroxide; diphenylphosphoranyl azide; triethylamine; In tetrahydrofuran; N,N-dimethyl-formamide; 1: Condensation / 2: Hydrolysis / 3: Condensation;
DOI:10.1246/bcsj.71.1159
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