N-(5-dimethylaminonaphthalenesulfonyl)-N'-(4-methoxybenzenesulfonyl)-bis(3-aminopropyl)cyclohexylmethylamine

Base Information

Chemical Name:N-(5-dimethylaminonaphthalenesulfonyl)-N'-(4-methoxybenzenesulfonyl)-bis(3-aminopropyl)cyclohexylmethylamine
CAS No.:1322645-20-4
Molecular Formula:C₃₂H₄₆N₄O₅S₂
Molecular Weight:630.873
Hs Code.:

Synonyms:N-(5-dimethylaminonaphthalenesulfonyl)-N'-(4-methoxybenzenesulfonyl)-bis(3-aminopropyl)cyclohexylmethylamine

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-(5-dimethylaminonaphthalenesulfonyl)-N'-(4-methoxybenzenesulfonyl)-bis(3-aminopropyl)cyclohexylmethylamine

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Technology Process of N-(5-dimethylaminonaphthalenesulfonyl)-N'-(4-methoxybenzenesulfonyl)-bis(3-aminopropyl)cyclohexylmethylamine

There total 5 articles about N-(5-dimethylaminonaphthalenesulfonyl)-N'-(4-methoxybenzenesulfonyl)-bis(3-aminopropyl)cyclohexylmethylamine 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: 69.0%

: 1094269-81-4
N-(3-bromo-propyl)-4-methoxy-benzenesulfonamide

: 1322645-00-0
N-(3-(5-dimethylaminonaphthalene-1-sulfonamidopropyl)cyclohexylmethyl)amine

: 1322645-20-4
N-(5-dimethylaminonaphthalenesulfonyl)-N'-(4-methoxybenzenesulfonyl)-bis(3-aminopropyl)cyclohexylmethylamine

Guidance literature:: With sodium carbonate; sodium iodide; In acetonitrile; for 24h; Inert atmosphere; Reflux;
DOI:10.1021/jm2002603

Reference yield:

: C₂₂H₃₁N₃O₂S

: 1322645-20-4
N-(5-dimethylaminonaphthalenesulfonyl)-N'-(4-methoxybenzenesulfonyl)-bis(3-aminopropyl)cyclohexylmethylamine

Guidance literature:: Multi-step reaction with 2 steps

1: sodium tetrahydroborate / ethanol / 12 h / 20 °C / Inert atmosphere

2: sodium carbonate; sodium iodide / acetonitrile / 24 h / Inert atmosphere; Reflux

With sodium tetrahydroborate; sodium carbonate; sodium iodide; In ethanol; acetonitrile;
DOI:10.1021/jm2002603

Reference yield:

: 605-65-2
5-(dimethylamino)naphth-1-ylsulfonyl chloride

: 1322645-20-4
N-(5-dimethylaminonaphthalenesulfonyl)-N'-(4-methoxybenzenesulfonyl)-bis(3-aminopropyl)cyclohexylmethylamine

Guidance literature:: Multi-step reaction with 4 steps

1: dichloromethane / 18 h / 20 °C / Inert atmosphere

2: magnesium sulfate / dichloromethane / 24 h / 20 °C / Inert atmosphere

3: sodium tetrahydroborate / ethanol / 12 h / 20 °C / Inert atmosphere

4: sodium carbonate; sodium iodide / acetonitrile / 24 h / Inert atmosphere; Reflux

With sodium tetrahydroborate; sodium carbonate; magnesium sulfate; sodium iodide; In ethanol; dichloromethane; acetonitrile;
DOI:10.1021/jm2002603