N-(2-iodophenyl)-N-tert-butoxycarbonyl-(1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)methanamine

Base Information

Chemical Name:N-(2-iodophenyl)-N-tert-butoxycarbonyl-(1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)methanamine
CAS No.:1059682-26-6
Molecular Formula:C₂₀H₂₀IN₅O₄
Molecular Weight:521.314
Hs Code.:

Synonyms:N-(2-iodophenyl)-N-tert-butoxycarbonyl-(1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)methanamine

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-(2-iodophenyl)-N-tert-butoxycarbonyl-(1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)methanamine

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Technology Process of N-(2-iodophenyl)-N-tert-butoxycarbonyl-(1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)methanamine

There total 1 articles about N-(2-iodophenyl)-N-tert-butoxycarbonyl-(1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)methanamine 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: 69.0%

: 947689-44-3
N-(2-iodophenyl)-N-tert-butoxycarbonyl-2-propynylamine

: 1516-60-5
4-nitrophenyl azide

: 1059682-26-6
N-(2-iodophenyl)-N-tert-butoxycarbonyl-(1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)methanamine

Guidance literature:: With copper(II) sulfate; sodium L-ascorbate; In water; tert-butyl alcohol; at 20 ℃; for 24h;
DOI:10.1016/j.tet.2008.06.042

Reference yield: 73.0%

: 1059682-26-6
N-(2-iodophenyl)-N-tert-butoxycarbonyl-(1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)methanamine

: 1059682-02-8
5-(tert-butoxycarbonyl)-1-(4-nitrophenyl)-[1,2,3]triazolo[4,5-c]quinoline

Guidance literature:: With tetrabutyl-ammonium chloride; potassium acetate; palladium diacetate; In N,N-dimethyl-formamide; at 120 ℃; for 1h; microwave irradiation;
DOI:10.1016/j.tet.2008.06.042