N-([1-(2-aminoethyl)-4-phenyl-1H-1,2,3-triazol-4-yl]methyl)-2-(4-chlorophenyl)diazenecarboxamide

Base Information

Chemical Name:N-([1-(2-aminoethyl)-4-phenyl-1H-1,2,3-triazol-4-yl]methyl)-2-(4-chlorophenyl)diazenecarboxamide
CAS No.:1224434-29-0
Molecular Formula:C₁₂H₁₄ClN₇O
Molecular Weight:307.742
Hs Code.:

Synonyms:N-([1-(2-aminoethyl)-4-phenyl-1H-1,2,3-triazol-4-yl]methyl)-2-(4-chlorophenyl)diazenecarboxamide

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Chemical Property of N-([1-(2-aminoethyl)-4-phenyl-1H-1,2,3-triazol-4-yl]methyl)-2-(4-chlorophenyl)diazenecarboxamide

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Technology Process of N-([1-(2-aminoethyl)-4-phenyl-1H-1,2,3-triazol-4-yl]methyl)-2-(4-chlorophenyl)diazenecarboxamide

There total 1 articles about N-([1-(2-aminoethyl)-4-phenyl-1H-1,2,3-triazol-4-yl]methyl)-2-(4-chlorophenyl)diazenecarboxamide 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:

Reference yield: 96.0%

: 87156-40-9
1-amino-2-azidoethane

: 1224434-03-0
2-(4-chlorophenyl)-N-(prop-2-ynyl)diazenecarboxamide

: 1224434-29-0
N-([1-(2-aminoethyl)-4-phenyl-1H-1,2,3-triazol-4-yl]methyl)-2-(4-chlorophenyl)diazenecarboxamide

Guidance literature:: With copper(ll) sulfate pentahydrate; copper; In methanol; water; at 20 ℃; for 0.0833333h; regioselective reaction;
DOI:10.1016/j.tet.2010.02.042

Reference yield: 55.0%

: 75992-73-3,25794-47-2,30729-25-0,15274-33-6,22840-91-1,14568-13-9
cis-dichlorobis(dimethylsulfoxide)platinum(II)

: 1224434-29-0
N-([1-(2-aminoethyl)-4-phenyl-1H-1,2,3-triazol-4-yl]methyl)-2-(4-chlorophenyl)diazenecarboxamide

: cis-[(N-([1-(2-aminoethyl)-4-phenyl-1H-1,2,3-triazol-4-yl]methyl)-2-(4-chlorophenyl)diazenecarboxamide)(dimethylsulfoxide)chloroplatinum(II)]

Guidance literature:: In acetonitrile; equimol., stirred in the dark for 17 d; not isolated, detected by NMR; Kinetics;
DOI:10.1002/ejic.201001051