ethyl 4-((1-((4-amino-2-methylpyrimidin-5-yl)methyl)-1H-1,2,3-triazol-4-yl)methoxy)benzoate

Base Information

Chemical Name:ethyl 4-((1-((4-amino-2-methylpyrimidin-5-yl)methyl)-1H-1,2,3-triazol-4-yl)methoxy)benzoate
CAS No.:1351982-03-0
Molecular Formula:C₁₈H₂₀N₆O₃
Molecular Weight:368.395
Hs Code.:

Synonyms:ethyl 4-((1-((4-amino-2-methylpyrimidin-5-yl)methyl)-1H-1,2,3-triazol-4-yl)methoxy)benzoate

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Chemical Property of ethyl 4-((1-((4-amino-2-methylpyrimidin-5-yl)methyl)-1H-1,2,3-triazol-4-yl)methoxy)benzoate

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Technology Process of ethyl 4-((1-((4-amino-2-methylpyrimidin-5-yl)methyl)-1H-1,2,3-triazol-4-yl)methoxy)benzoate

There total 4 articles about ethyl 4-((1-((4-amino-2-methylpyrimidin-5-yl)methyl)-1H-1,2,3-triazol-4-yl)methoxy)benzoate 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: 94.0%

: 175203-55-1
4-prop-2-ynyloxybenzoic acid ethyl ester

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

: 1351982-03-0
ethyl 4-((1-((4-amino-2-methylpyrimidin-5-yl)methyl)-1H-1,2,3-triazol-4-yl)methoxy)benzoate

Guidance literature:: With copper(ll) sulfate pentahydrate; sodium L-ascorbate; In water; tert-butyl alcohol; at 20 ℃; for 12h;
DOI:10.1016/j.bmc.2011.10.035

Reference yield: 94.0%

: 1351982-03-0
ethyl 4-((1-((4-amino-2-methylpyrimidin-5-yl)methyl)-1H-1,2,3-triazol-4-yl)methoxy)benzoate

Guidance literature:: With copper(ll) sulfate pentahydrate; sodium L-ascorbate; In water; tert-butyl alcohol; at 60 - 70 ℃;

Reference yield:

: 70-16-6
Aneurin

: 1351982-03-0
ethyl 4-((1-((4-amino-2-methylpyrimidin-5-yl)methyl)-1H-1,2,3-triazol-4-yl)methoxy)benzoate

Guidance literature:: Multi-step reaction with 2 steps

1: sodium azide; sodium sulfite / water / 6 h / 60 - 65 °C

2: copper(ll) sulfate pentahydrate; sodium L-ascorbate / water; tert-butyl alcohol / 12 h / 20 °C

With sodium azide; copper(ll) sulfate pentahydrate; sodium L-ascorbate; sodium sulfite; In water; tert-butyl alcohol;
DOI:10.1016/j.bmc.2011.10.035