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5-amino-1-(2',3'-O-isopropylidene-4'-hydroxymethylcyclopentyl)imidazole-4-dibenzyl aspartyl carboxamide

Base Information Edit
  • Chemical Name:5-amino-1-(2',3'-O-isopropylidene-4'-hydroxymethylcyclopentyl)imidazole-4-dibenzyl aspartyl carboxamide
  • CAS No.:174088-42-7
  • Molecular Formula:C31H36N4O8
  • Molecular Weight:592.649
  • Hs Code.:
  • Mol file:174088-42-7.mol
5-amino-1-(2',3'-O-isopropylidene-4'-hydroxymethylcyclopentyl)imidazole-4-dibenzyl aspartyl carboxamide

Synonyms:

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Chemical Property of 5-amino-1-(2',3'-O-isopropylidene-4'-hydroxymethylcyclopentyl)imidazole-4-dibenzyl aspartyl carboxamide Edit
Chemical Property:
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Technology Process of 5-amino-1-(2',3'-O-isopropylidene-4'-hydroxymethylcyclopentyl)imidazole-4-dibenzyl aspartyl carboxamide

There total 10 articles about 5-amino-1-(2',3'-O-isopropylidene-4'-hydroxymethylcyclopentyl)imidazole-4-dibenzyl aspartyl carboxamide 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 5 steps
1: 97 percent / SnCl2, thiophenol, Et3N / CH2Cl2 / 1.) 0 deg C, 30 min, 2.) 25 deg C, 18 h
2: 96 percent / TBAF / tetrahydrofuran; H2O / 1 h / 25 °C
3: 43 percent / acetonitrile / 19 h / 25 °C
4: H2 / Pd/C / aq. ethanol / 4 h / 760 Torr
5: CF3-HOBT, DCC / acetonitrile / 17 h / 25 °C
With CF3-HOBT; tetrabutyl ammonium fluoride; hydrogen; thiophenol; triethylamine; dicyclohexyl-carbodiimide; tin(ll) chloride; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane; water; acetonitrile;
DOI:10.1080/15257779508010715
Guidance literature:
Multi-step reaction with 4 steps
1: 96 percent / TBAF / tetrahydrofuran; H2O / 1 h / 25 °C
2: 43 percent / acetonitrile / 19 h / 25 °C
3: H2 / Pd/C / aq. ethanol / 4 h / 760 Torr
4: CF3-HOBT, DCC / acetonitrile / 17 h / 25 °C
With CF3-HOBT; tetrabutyl ammonium fluoride; hydrogen; dicyclohexyl-carbodiimide; palladium on activated charcoal; In tetrahydrofuran; ethanol; water; acetonitrile;
DOI:10.1080/15257779508010715
Guidance literature:
Multi-step reaction with 7 steps
1: DMAP / pyridine / 2 h / 0 °C
2: NaN3 / dimethylformamide / 1.) 0 deg C, 1 h, 2.) 25 deg C, 15 h
3: 97 percent / SnCl2, thiophenol, Et3N / CH2Cl2 / 1.) 0 deg C, 30 min, 2.) 25 deg C, 18 h
4: 96 percent / TBAF / tetrahydrofuran; H2O / 1 h / 25 °C
5: 43 percent / acetonitrile / 19 h / 25 °C
6: H2 / Pd/C / aq. ethanol / 4 h / 760 Torr
7: CF3-HOBT, DCC / acetonitrile / 17 h / 25 °C
With dmap; sodium azide; CF3-HOBT; tetrabutyl ammonium fluoride; hydrogen; thiophenol; triethylamine; dicyclohexyl-carbodiimide; tin(ll) chloride; palladium on activated charcoal; In tetrahydrofuran; pyridine; ethanol; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1080/15257779508010715
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