N-[1-{3-[4-(3-diallylamino-propylamino)-butoxy]-propylcarbamoyl}-2-(4-hydroxy-phenyl)-ethyl]-butyramide

Base Information

Chemical Name:N-[1-{3-[4-(3-diallylamino-propylamino)-butoxy]-propylcarbamoyl}-2-(4-hydroxy-phenyl)-ethyl]-butyramide
CAS No.:252897-38-4
Molecular Formula:C₂₉H₄₈N₄O₄
Molecular Weight:516.725
Hs Code.:

<i>N</i>-[1-{3-[4-(3-diallylamino-propylamino)-butoxy]-propylcarbamoyl}-2-(4-hydroxy-phenyl)-ethyl]-butyramide

Synonyms:N-[1-{3-[4-(3-diallylamino-propylamino)-butoxy]-propylcarbamoyl}-2-(4-hydroxy-phenyl)-ethyl]-butyramide

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Chemical Property of N-[1-{3-[4-(3-diallylamino-propylamino)-butoxy]-propylcarbamoyl}-2-(4-hydroxy-phenyl)-ethyl]-butyramide

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Technology Process of N-[1-{3-[4-(3-diallylamino-propylamino)-butoxy]-propylcarbamoyl}-2-(4-hydroxy-phenyl)-ethyl]-butyramide

There total 6 articles about N-[1-{3-[4-(3-diallylamino-propylamino)-butoxy]-propylcarbamoyl}-2-(4-hydroxy-phenyl)-ethyl]-butyramide 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: 44.0%

: 252897-30-6
(R,S)-N-(1-oxobutyl)tyrosine

: 252897-34-0
N,N-di(2-propenyl)-N'-[4-(3-aminopropyloxy)butyl]-1,3-propanediamine

: 252897-38-4
N-[1-{3-[4-(3-diallylamino-propylamino)-butoxy]-propylcarbamoyl}-2-(4-hydroxy-phenyl)-ethyl]-butyramide

Guidance literature:: (R,S)-N-(1-oxobutyl)tyrosine; With dicyclohexyl-carbodiimide; In 1,2-dimethoxyethane; dichloromethane; at 20 ℃; for 0.5h;

N,N-di(2-propenyl)-N'-[4-(3-aminopropyloxy)butyl]-1,3-propanediamine; In dichloromethane; at 20 ℃; for 20h;
DOI:10.1021/jm9903747

Reference yield:

: 18642-17-6
3-(4-hydroxybutyloxy)propanenitrile

: 252897-38-4
N-[1-{3-[4-(3-diallylamino-propylamino)-butoxy]-propylcarbamoyl}-2-(4-hydroxy-phenyl)-ethyl]-butyramide

Guidance literature:: Multi-step reaction with 4 steps

1.1: 82 percent / methyltriphenylphosphonium iodide / CH₂Cl₂ / 1 h / 20 °C

2.1: NaH / dimethylformamide / 0.75 h / 20 °C

2.2: 40 percent / dimethylformamide / 2 h / 20 °C

3.1: 84 percent / LiAlH₄ / diethyl ether / 4 h / 0 - 20 °C

4.1: dicyclohexylcarbodiimide / 1,2-dimethoxy-ethane; CH₂Cl₂ / 0.5 h / 20 °C

4.2: 44 percent / CH₂Cl₂ / 20 h / 20 °C

With lithium aluminium tetrahydride; methyl-triphenylphosphonium iodide; sodium hydride; dicyclohexyl-carbodiimide; In 1,2-dimethoxyethane; diethyl ether; dichloromethane; N,N-dimethyl-formamide; 1.1: Iodination / 2.1: Metallation / 2.2: Alkylation / 3.1: Reduction / 4.1: Esterification / 4.2: Condensation;
DOI:10.1021/jm9903747

Reference yield:

: 556-02-5,556-03-6,34537-57-0,55520-40-6,96946-98-4,60-18-4,18875-48-4,25619-78-7,30704-25-7
?Tyr

: 252897-38-4
N-[1-{3-[4-(3-diallylamino-propylamino)-butoxy]-propylcarbamoyl}-2-(4-hydroxy-phenyl)-ethyl]-butyramide

Guidance literature:: Multi-step reaction with 2 steps

1.1: 56 percent / aq. NaOH / tetrahydrofuran

2.1: dicyclohexylcarbodiimide / 1,2-dimethoxy-ethane; CH₂Cl₂ / 0.5 h / 20 °C

2.2: 44 percent / CH₂Cl₂ / 20 h / 20 °C

With sodium hydroxide; dicyclohexyl-carbodiimide; In tetrahydrofuran; 1,2-dimethoxyethane; dichloromethane; 1.1: Acylation / 2.1: Esterification / 2.2: Condensation;
DOI:10.1021/jm9903747