(1-((4-amino-2-methylpyrimidin-5-yl)methyl)-5-iodo-1H-1,2,3-triazol-4-yl)methyl-4-methylbenzoate

Base Information

Chemical Name:(1-((4-amino-2-methylpyrimidin-5-yl)methyl)-5-iodo-1H-1,2,3-triazol-4-yl)methyl-4-methylbenzoate
CAS No.:1428140-91-3
Molecular Formula:C₁₇H₁₇IN₆O₂
Molecular Weight:464.265
Hs Code.:

Synonyms:(1-((4-amino-2-methylpyrimidin-5-yl)methyl)-5-iodo-1H-1,2,3-triazol-4-yl)methyl-4-methylbenzoate

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Chemical Property of (1-((4-amino-2-methylpyrimidin-5-yl)methyl)-5-iodo-1H-1,2,3-triazol-4-yl)methyl-4-methylbenzoate

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Technology Process of (1-((4-amino-2-methylpyrimidin-5-yl)methyl)-5-iodo-1H-1,2,3-triazol-4-yl)methyl-4-methylbenzoate

There total 6 articles about (1-((4-amino-2-methylpyrimidin-5-yl)methyl)-5-iodo-1H-1,2,3-triazol-4-yl)methyl-4-methylbenzoate 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: 75.0%

: 3-p-methylbenzoyloxy-1-iodo-1-propyne

: 63423-50-7
5‐(azidomethyl)‐2‐methylpyrimidin‐4‐amine

: 1428140-91-3
(1-((4-amino-2-methylpyrimidin-5-yl)methyl)-5-iodo-1H-1,2,3-triazol-4-yl)methyl-4-methylbenzoate

Guidance literature:: With copper(l) iodide; triethylamine; In tetrahydrofuran; at 20 ℃; for 12h;
DOI:10.1016/j.bmc.2019.01.021

Reference yield: 75.0%

: 1428140-91-3
(1-((4-amino-2-methylpyrimidin-5-yl)methyl)-5-iodo-1H-1,2,3-triazol-4-yl)methyl-4-methylbenzoate

Guidance literature:: With copper(l) iodide; triethylamine; In acetonitrile; at 40 - 50 ℃; for 12h;

Reference yield:

: 99-94-5
p-Toluic acid

: 1428140-91-3
(1-((4-amino-2-methylpyrimidin-5-yl)methyl)-5-iodo-1H-1,2,3-triazol-4-yl)methyl-4-methylbenzoate

Guidance literature:: Multi-step reaction with 4 steps

1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 20 °C

2: trialkylamine / dichloromethane / 0 - 20 °C

3: copper(l) iodide; N-iodomorpholine / tetrahydrofuran / 1 h / 20 °C

4: triethylamine; copper(l) iodide / tetrahydrofuran / 12 h / 20 °C

With N-iodomorpholine; copper(l) iodide; oxalyl dichloride; triethylamine; N,N-dimethyl-formamide; In tetrahydrofuran; dichloromethane;
DOI:10.1016/j.bmc.2019.01.021