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2-methyl-N-(3-morpholino-3-oxopropyl)-4-phenyl-4H-benzo[4,5]thiazolo[3,2-a]pyri midine-3-carboxamide

Base Information
  • Chemical Name:2-methyl-N-(3-morpholino-3-oxopropyl)-4-phenyl-4H-benzo[4,5]thiazolo[3,2-a]pyri midine-3-carboxamide
  • CAS No.:1489134-82-8
  • Molecular Formula:C25H26N4O3S
  • Molecular Weight:462.572
  • Hs Code.:
2-methyl-N-(3-morpholino-3-oxopropyl)-4-phenyl-4H-benzo[4,5]thiazolo[3,2-a]pyri midine-3-carboxamide

Synonyms:2-methyl-N-(3-morpholino-3-oxopropyl)-4-phenyl-4H-benzo[4,5]thiazolo[3,2-a]pyri midine-3-carboxamide

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Chemical Property of 2-methyl-N-(3-morpholino-3-oxopropyl)-4-phenyl-4H-benzo[4,5]thiazolo[3,2-a]pyri midine-3-carboxamide
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Technology Process of 2-methyl-N-(3-morpholino-3-oxopropyl)-4-phenyl-4H-benzo[4,5]thiazolo[3,2-a]pyri midine-3-carboxamide

There total 6 articles about 2-methyl-N-(3-morpholino-3-oxopropyl)-4-phenyl-4H-benzo[4,5]thiazolo[3,2-a]pyri midine-3-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:
3-(2-methyl-4-phenyl-4H-benzo[4,5]thiazolo[3,2-a]pyrimidine-3-carboxamido)propanoic acid; With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; for 0.0833333h; Inert atmosphere;
morpholine; With triethylamine; In dichloromethane; at 20 ℃; for 1h; Inert atmosphere;
DOI:10.1016/j.ejmech.2013.08.024
Guidance literature:
Multi-step reaction with 3 steps
1.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 0.08 h / Inert atmosphere
1.2: 2 h / 20 °C / Inert atmosphere
2.1: potassium hydroxide / ethanol / 1 h / Reflux
3.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 0.08 h / Inert atmosphere
3.2: 1 h / 20 °C / Inert atmosphere
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; potassium hydroxide; In ethanol; dichloromethane;
DOI:10.1016/j.ejmech.2013.08.024
Guidance literature:
Multi-step reaction with 4 steps
1.1: potassium hydroxide / ethanol / 2 h / Reflux
2.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 0.08 h / Inert atmosphere
2.2: 2 h / 20 °C / Inert atmosphere
3.1: potassium hydroxide / ethanol / 1 h / Reflux
4.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 0.08 h / Inert atmosphere
4.2: 1 h / 20 °C / Inert atmosphere
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; potassium hydroxide; In ethanol; dichloromethane;
DOI:10.1016/j.ejmech.2013.08.024
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