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3-(2,5-dichloro-4-(((2S,4S)-2-(4-cyclopropyl-1,2,3,4-tetrahydroquinoxaline-1-carbonyl)-4-fluoropyrrolidin-1-yl)methyl)phenyl)-N-((2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl)propanamide

Base Information
  • Chemical Name:3-(2,5-dichloro-4-(((2S,4S)-2-(4-cyclopropyl-1,2,3,4-tetrahydroquinoxaline-1-carbonyl)-4-fluoropyrrolidin-1-yl)methyl)phenyl)-N-((2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl)propanamide
  • CAS No.:1445984-46-2
  • Molecular Formula:C32H41Cl2FN4O7
  • Molecular Weight:683.605
  • Hs Code.:
3-(2,5-dichloro-4-(((2S,4S)-2-(4-cyclopropyl-1,2,3,4-tetrahydroquinoxaline-1-carbonyl)-4-fluoropyrrolidin-1-yl)methyl)phenyl)-N-((2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl)propanamide

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Chemical Property of 3-(2,5-dichloro-4-(((2S,4S)-2-(4-cyclopropyl-1,2,3,4-tetrahydroquinoxaline-1-carbonyl)-4-fluoropyrrolidin-1-yl)methyl)phenyl)-N-((2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl)propanamide
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Technology Process of 3-(2,5-dichloro-4-(((2S,4S)-2-(4-cyclopropyl-1,2,3,4-tetrahydroquinoxaline-1-carbonyl)-4-fluoropyrrolidin-1-yl)methyl)phenyl)-N-((2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl)propanamide

There total 8 articles about 3-(2,5-dichloro-4-(((2S,4S)-2-(4-cyclopropyl-1,2,3,4-tetrahydroquinoxaline-1-carbonyl)-4-fluoropyrrolidin-1-yl)methyl)phenyl)-N-((2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl)propanamide 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 N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1021/acs.jmedchem.8b00308
Guidance literature:
Multi-step reaction with 8 steps
1: acetic acid; acetic anhydride; sulfuric acid; chromium(VI) oxide / 6 h / 0 - 20 °C
2: sodium hydroxide / dichloromethane; water / 1 h / 0 °C
3: sodium tetrahydroborate / methanol / 1 h / 20 °C
4: hydrogen; rhodium contaminated with carbon / ethyl acetate / 20 °C
5: triphenylphosphine; N-Bromosuccinimide / dichloromethane; tetrahydrofuran / 2 h / 0 °C
6: potassium carbonate / acetonitrile / 20 °C
7: trimethylsilyl bromide / dichloromethane / 2 h / 20 °C
8: N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / N,N-dimethyl-formamide / 20 °C
With chromium(VI) oxide; sodium tetrahydroborate; N-Bromosuccinimide; trimethylsilyl bromide; sulfuric acid; rhodium contaminated with carbon; hydrogen; acetic anhydride; potassium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; triphenylphosphine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; sodium hydroxide; In tetrahydrofuran; methanol; dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/acs.jmedchem.8b00308
Guidance literature:
Multi-step reaction with 2 steps
1: trimethylsilyl bromide / dichloromethane / 2 h / 20 °C
2: N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / N,N-dimethyl-formamide / 20 °C
With trimethylsilyl bromide; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/acs.jmedchem.8b00308
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