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(2R,3S)-3-(cyclopropylmethyl)-N1-((R)-9-fluoro-2-oxo-5-phenyl-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-yl)-2-(3,3,3-trifluoropropyl)succinamide

Base Information
  • Chemical Name:(2R,3S)-3-(cyclopropylmethyl)-N1-((R)-9-fluoro-2-oxo-5-phenyl-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-yl)-2-(3,3,3-trifluoropropyl)succinamide
  • CAS No.:1584715-30-9
  • Molecular Formula:C26H26F4N4O3
  • Molecular Weight:518.511
  • Hs Code.:
(2R,3S)-3-(cyclopropylmethyl)-N<sub>1</sub>-((R)-9-fluoro-2-oxo-5-phenyl-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-yl)-2-(3,3,3-trifluoropropyl)succinamide

Synonyms:(2R,3S)-3-(cyclopropylmethyl)-N1-((R)-9-fluoro-2-oxo-5-phenyl-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-yl)-2-(3,3,3-trifluoropropyl)succinamide

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Chemical Property of (2R,3S)-3-(cyclopropylmethyl)-N1-((R)-9-fluoro-2-oxo-5-phenyl-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-yl)-2-(3,3,3-trifluoropropyl)succinamide
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Technology Process of (2R,3S)-3-(cyclopropylmethyl)-N1-((R)-9-fluoro-2-oxo-5-phenyl-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-yl)-2-(3,3,3-trifluoropropyl)succinamide

There total 17 articles about (2R,3S)-3-(cyclopropylmethyl)-N1-((R)-9-fluoro-2-oxo-5-phenyl-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-yl)-2-(3,3,3-trifluoropropyl)succinamide 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:
C30H33F4N3O4; With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 1.83333h;
With ammonia; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; isopropyl alcohol; at 8 - 20 ℃;
In methanol; carbon dioxide; at 40 ℃; under 75007.5 Torr; Supercritical conditions; liquid CO2;
Guidance literature:
Multi-step reaction with 4 steps
1.1: oxalyl dichloride / N,N-dimethyl-formamide; tetrahydrofuran / 1.5 h / 0 °C
1.2: 20 °C
2.1: hydrogen bromide; acetic acid / 1.5 h / 20 °C
3.1: triethylamine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / N,N-dimethyl-formamide / 1.5 h / 20 °C
4.1: trifluoroacetic acid / dichloromethane / 1.83 h / 20 °C
4.2: 8 - 20 °C
4.3: Lux-Cell4 / 40 °C / 75007.5 Torr / Supercritical conditions; liquid CO2
With oxalyl dichloride; hydrogen bromide; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; acetic acid; triethylamine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
Guidance literature:
Multi-step reaction with 5 steps
1.1: potassium hexacyanoferrate(II); sodium hydrogencarbonate; sodium hydroxide / N,N-dimethyl-formamide; water / 1.67 h / 110 - 120 °C
2.1: oxalyl dichloride / N,N-dimethyl-formamide; tetrahydrofuran / 1.5 h / 0 °C
2.2: 20 °C
3.1: hydrogen bromide; acetic acid / 1.5 h / 20 °C
4.1: triethylamine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / N,N-dimethyl-formamide / 1.5 h / 20 °C
5.1: trifluoroacetic acid / dichloromethane / 1.83 h / 20 °C
5.2: 8 - 20 °C
5.3: Lux-Cell4 / 40 °C / 75007.5 Torr / Supercritical conditions; liquid CO2
With potassium hexacyanoferrate(II); oxalyl dichloride; hydrogen bromide; sodium hydrogencarbonate; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; acetic acid; triethylamine; trifluoroacetic acid; sodium hydroxide; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide;
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