N-(2-(diethylamino)ethyl)-2-(((2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl)thio)benzamide

Base Information

Chemical Name:N-(2-(diethylamino)ethyl)-2-(((2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl)thio)benzamide
CAS No.:1611453-61-2
Molecular Formula:C₂₈H₄₄N₂OS
Molecular Weight:456.736
Hs Code.:

Synonyms:N-(2-(diethylamino)ethyl)-2-(((2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl)thio)benzamide

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Chemical Property of N-(2-(diethylamino)ethyl)-2-(((2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl)thio)benzamide

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Technology Process of N-(2-(diethylamino)ethyl)-2-(((2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl)thio)benzamide

There total 7 articles about N-(2-(diethylamino)ethyl)-2-(((2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl)thio)benzamide 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: 78.0%

: 2-(((2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl)thio)-benzoyl chloride

: 100-36-7
N,N-diethylethylenediamine

: 1611453-61-2
N-(2-(diethylamino)ethyl)-2-(((2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl)thio)benzamide

Guidance literature:: With triethylamine; In dichloromethane; at 0 ℃; for 0.5h;
DOI:10.1002/ardp.201300325

Reference yield:

: methyl 2-(((2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl)thio)benzoate

: 1611453-61-2
N-(2-(diethylamino)ethyl)-2-(((2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl)thio)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydroxide / methanol; water / 10 h / 60 °C

2: oxalyl dichloride / dichloromethane / 4 h / 20 °C

3: triethylamine / dichloromethane / 0.5 h / 0 °C

With oxalyl dichloride; triethylamine; sodium hydroxide; In methanol; dichloromethane; water;
DOI:10.1002/ardp.201300325

Reference yield:

: 24163-93-7,24163-94-8,56881-57-3,6874-67-5,28290-41-7
farnesyl bromide

: 1611453-61-2
N-(2-(diethylamino)ethyl)-2-(((2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl)thio)benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / acetonitrile / 6 h / Reflux

2: sodium hydroxide / methanol; water / 10 h / 60 °C

3: oxalyl dichloride / dichloromethane / 4 h / 20 °C

4: triethylamine / dichloromethane / 0.5 h / 0 °C

With oxalyl dichloride; potassium carbonate; triethylamine; sodium hydroxide; In methanol; dichloromethane; water; acetonitrile;
DOI:10.1002/ardp.201300325