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C21H19N5O3

Base Information
  • Chemical Name:C21H19N5O3
  • CAS No.:1569316-89-7
  • Molecular Formula:C21H19N5O3
  • Molecular Weight:389.414
  • Hs Code.:
C<sub>21</sub>H<sub>19</sub>N<sub>5</sub>O<sub>3</sub>

Synonyms:

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Chemical Property of C21H19N5O3
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Technology Process of C21H19N5O3

There total 3 articles about C21H19N5O3 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:
C22H21N5O3; With lithium hydroxide; In methanol; water; at 20 ℃; for 4h; Sealed tube;
With acetic acid; In methanol; water; Sealed tube;
DOI:10.1021/jm401848a
Guidance literature:
Multi-step reaction with 3 steps
1.1: thionyl chloride / 23 h / Reflux
2.1: 1-[(1-(cyano-?2-?ethoxy-?2-?oxoethylidenaminooxy)?dimethylamino-?morpholino)]-uronium hexafluorophosphate; triethylamine / N,N-dimethyl-formamide / 21 h / Sealed tube
3.1: lithium hydroxide / water; methanol / 4 h / 20 °C / Sealed tube
3.2: Sealed tube
With thionyl chloride; 1-[(1-(cyano-?2-?ethoxy-?2-?oxoethylidenaminooxy)?dimethylamino-?morpholino)]-uronium hexafluorophosphate; triethylamine; lithium hydroxide; In methanol; water; N,N-dimethyl-formamide;
DOI:10.1021/jm401848a
Guidance literature:
Multi-step reaction with 2 steps
1.1: 1-[(1-(cyano-?2-?ethoxy-?2-?oxoethylidenaminooxy)?dimethylamino-?morpholino)]-uronium hexafluorophosphate; triethylamine / N,N-dimethyl-formamide / 21 h / Sealed tube
2.1: lithium hydroxide / water; methanol / 4 h / 20 °C / Sealed tube
2.2: Sealed tube
With 1-[(1-(cyano-?2-?ethoxy-?2-?oxoethylidenaminooxy)?dimethylamino-?morpholino)]-uronium hexafluorophosphate; triethylamine; lithium hydroxide; In methanol; water; N,N-dimethyl-formamide;
DOI:10.1021/jm401848a
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