5-adamantan-1-yl-N-(3,4-dihydroxybenzyl)-2,4-dihydroxy-benzoic acid amide

Base Information

Chemical Name:5-adamantan-1-yl-N-(3,4-dihydroxybenzyl)-2,4-dihydroxy-benzoic acid amide
CAS No.:1422043-80-8
Molecular Formula:C₂₄H₂₇NO₅
Molecular Weight:409.482
Hs Code.:

Synonyms:5-adamantan-1-yl-N-(3,4-dihydroxybenzyl)-2,4-dihydroxy-benzoic acid amide

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Chemical Property of 5-adamantan-1-yl-N-(3,4-dihydroxybenzyl)-2,4-dihydroxy-benzoic acid amide

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Technology Process of 5-adamantan-1-yl-N-(3,4-dihydroxybenzyl)-2,4-dihydroxy-benzoic acid amide

There total 6 articles about 5-adamantan-1-yl-N-(3,4-dihydroxybenzyl)-2,4-dihydroxy-benzoic acid amide 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:

: C₂₁H₂₃NO₆

: 1124-40-9
3,4-dihydroxybenzylamine hydrochloride

: 1422043-80-8
5-adamantan-1-yl-N-(3,4-dihydroxybenzyl)-2,4-dihydroxy-benzoic acid amide

Guidance literature:: With sodium hydrogencarbonate; In water; at 60 ℃; Inert atmosphere;
DOI:10.1016/j.bmcl.2013.11.056

Reference yield:

: 37491-68-2
3,4-dihydroxybenzylamine

: 51049-71-9
5-adamantan-1-yl-2,4-dihydroxybenzoic acid

: 1422043-80-8
5-adamantan-1-yl-N-(3,4-dihydroxybenzyl)-2,4-dihydroxy-benzoic acid amide

Guidance literature:: 5-adamantan-1-yl-2,4-dihydroxybenzoic acid; With 1-hydroxy-pyrrolidine-2,5-dione; dicyclohexyl-carbodiimide; In 1,4-dioxane; for 12h;

3,4-dihydroxybenzylamine; With sodium hydrogencarbonate; In 1,4-dioxane; water; at 50 ℃; for 2h;

Reference yield:

: 89-86-1
4-hydroxysalicylic acid

: 1422043-80-8
5-adamantan-1-yl-N-(3,4-dihydroxybenzyl)-2,4-dihydroxy-benzoic acid amide

Guidance literature:: Multi-step reaction with 3 steps

1: sulfuric acid; acetic acid / dichloromethane / 20 °C

2: dicyclohexyl-carbodiimide / 1,4-dioxane / 12 h / 20 °C / Inert atmosphere

3: sodium hydrogencarbonate / water / 60 °C / Inert atmosphere

With sulfuric acid; sodium hydrogencarbonate; acetic acid; dicyclohexyl-carbodiimide; In 1,4-dioxane; dichloromethane; water;
DOI:10.1016/j.bmcl.2013.11.056