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C14H17N3O5

Base Information
  • Chemical Name:C14H17N3O5
  • CAS No.:1325238-19-4
  • Molecular Formula:C14H17N3O5
  • Molecular Weight:307.306
  • Hs Code.:
C<sub>14</sub>H<sub>17</sub>N<sub>3</sub>O<sub>5</sub>

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Chemical Property of C14H17N3O5
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Technology Process of C14H17N3O5

There total 3 articles about C14H17N3O5 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-[1-(4-methoxyphenylcarbamoyl)ethylcarbamoyl]acrylic acid; With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; In N,N-dimethyl-formamide; for 2h; Inert atmosphere;
With O-2-tetrahydro-2H-pyranhydroxylamine; In N,N-dimethyl-formamide; at 20 ℃; for 120h; Inert atmosphere;
DOI:10.1155/2011/403129
Guidance literature:
Multi-step reaction with 5 steps
1.1: diphenyl phosphoryl azide; triethylamine / N,N-dimethyl-formamide / 20 °C / Inert atmosphere
2.1: trifluoroacetic acid / 2 h / 20 °C / Inert atmosphere
3.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 1 h / 20 °C / Inert atmosphere
4.1: lithium hydroxide / methanol; water / 2 h / 20 °C / Inert atmosphere
4.2: amberlite IRN-77
5.1: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine / N,N-dimethyl-formamide / 2 h / Inert atmosphere
5.2: 120 h / 20 °C / Inert atmosphere
With diphenyl phosphoryl azide; benzotriazol-1-ol; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; trifluoroacetic acid; lithium hydroxide; In methanol; water; N,N-dimethyl-formamide;
DOI:10.1155/2011/403129
Guidance literature:
Multi-step reaction with 4 steps
1.1: trifluoroacetic acid / 2 h / 20 °C / Inert atmosphere
2.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 1 h / 20 °C / Inert atmosphere
3.1: lithium hydroxide / methanol; water / 2 h / 20 °C / Inert atmosphere
3.2: amberlite IRN-77
4.1: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine / N,N-dimethyl-formamide / 2 h / Inert atmosphere
4.2: 120 h / 20 °C / Inert atmosphere
With benzotriazol-1-ol; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; trifluoroacetic acid; lithium hydroxide; In methanol; water; N,N-dimethyl-formamide;
DOI:10.1155/2011/403129
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