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(4S)-3-<(2R)-2-(N-Benzylamino)propionyl>-4-(tert-butoxymethyl)-1-methyl-2-oxoimidazolidine

Base Information Edit
  • Chemical Name:(4S)-3-<(2R)-2-(N-Benzylamino)propionyl>-4-(tert-butoxymethyl)-1-methyl-2-oxoimidazolidine
  • CAS No.:168292-68-0
  • Molecular Formula:C19H29N3O3
  • Molecular Weight:347.458
  • Hs Code.:
  • Mol file:168292-68-0.mol
(4S)-3-<(2R)-2-(N-Benzylamino)propionyl>-4-(tert-butoxymethyl)-1-methyl-2-oxoimidazolidine

Synonyms:

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Chemical Property of (4S)-3-<(2R)-2-(N-Benzylamino)propionyl>-4-(tert-butoxymethyl)-1-methyl-2-oxoimidazolidine Edit
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Technology Process of (4S)-3-<(2R)-2-(N-Benzylamino)propionyl>-4-(tert-butoxymethyl)-1-methyl-2-oxoimidazolidine

There total 6 articles about (4S)-3-<(2R)-2-(N-Benzylamino)propionyl>-4-(tert-butoxymethyl)-1-methyl-2-oxoimidazolidine 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 6 steps
1: 73 percent / 4 N aq. HCl / dioxane / 6 h / Ambient temperature
2: BMS / tetrahydrofuran / 1.) r.t., 2 h, 2.) reflux, 2 h
3: H2SO4 / CH2Cl2 / Ambient temperature
4: 93 percent / H2 / 10percent Pd/C / methanol / 3 h / Ambient temperature
5: 70 percent / t-BuOK / tetrahydrofuran / 1.) -50 deg C, 20 min, 2.) -30 deg C, 30 min
6: K2CO3 / hexamethylphosphoric acid triamide / 14 h / 25 °C
With hydrogenchloride; dimethylsulfide borane complex; sulfuric acid; potassium tert-butylate; hydrogen; potassium carbonate; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; methanol; N,N,N,N,N,N-hexamethylphosphoric triamide; dichloromethane;
DOI:10.1021/jo00126a029
Guidance literature:
Multi-step reaction with 4 steps
1: H2SO4 / CH2Cl2 / Ambient temperature
2: 93 percent / H2 / 10percent Pd/C / methanol / 3 h / Ambient temperature
3: 70 percent / t-BuOK / tetrahydrofuran / 1.) -50 deg C, 20 min, 2.) -30 deg C, 30 min
4: K2CO3 / hexamethylphosphoric acid triamide / 14 h / 25 °C
With sulfuric acid; potassium tert-butylate; hydrogen; potassium carbonate; palladium on activated charcoal; In tetrahydrofuran; methanol; N,N,N,N,N,N-hexamethylphosphoric triamide; dichloromethane;
DOI:10.1021/jo00126a029
Guidance literature:
Multi-step reaction with 5 steps
1: BMS / tetrahydrofuran / 1.) r.t., 2 h, 2.) reflux, 2 h
2: H2SO4 / CH2Cl2 / Ambient temperature
3: 93 percent / H2 / 10percent Pd/C / methanol / 3 h / Ambient temperature
4: 70 percent / t-BuOK / tetrahydrofuran / 1.) -50 deg C, 20 min, 2.) -30 deg C, 30 min
5: K2CO3 / hexamethylphosphoric acid triamide / 14 h / 25 °C
With dimethylsulfide borane complex; sulfuric acid; potassium tert-butylate; hydrogen; potassium carbonate; palladium on activated charcoal; In tetrahydrofuran; methanol; N,N,N,N,N,N-hexamethylphosphoric triamide; dichloromethane;
DOI:10.1021/jo00126a029
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