N,N'-bis(tert-butyoxycarbonyl)-N''-(4-chlorobenzyl)-N''-(5-pyrrolidin-1-yl-pentyl)-guanidine

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Chemical Name:N,N'-bis(tert-butyoxycarbonyl)-N''-(4-chlorobenzyl)-N''-(5-pyrrolidin-1-yl-pentyl)-guanidine
CAS No.:239482-90-7
Molecular Formula:C₂₇H₄₃ClN₄O₄
Molecular Weight:523.116
Hs Code.:

Synonyms:N,N'-bis(tert-butyoxycarbonyl)-N''-(4-chlorobenzyl)-N''-(5-pyrrolidin-1-yl-pentyl)-guanidine

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Chemical Property of N,N'-bis(tert-butyoxycarbonyl)-N''-(4-chlorobenzyl)-N''-(5-pyrrolidin-1-yl-pentyl)-guanidine

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Technology Process of N,N'-bis(tert-butyoxycarbonyl)-N''-(4-chlorobenzyl)-N''-(5-pyrrolidin-1-yl-pentyl)-guanidine

There total 7 articles about N,N'-bis(tert-butyoxycarbonyl)-N''-(4-chlorobenzyl)-N''-(5-pyrrolidin-1-yl-pentyl)-guanidine 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:

: 322474-21-5
N,N'-bis-Boc-S-methyl-isothiourea

: (4-chlorobenzyl)-(5-pyrrolidin-1-yl-pentyl)-amine bis-hydrochloride

: 239482-90-7
N,N'-bis(tert-butyoxycarbonyl)-N''-(4-chlorobenzyl)-N''-(5-pyrrolidin-1-yl-pentyl)-guanidine

Guidance literature:: With triethylamine; mercury dichloride; In dichloromethane; at 0 - 20 ℃; for 18h;
DOI:10.1021/jm990952j

Reference yield:

: 111-24-0
1,5-dibromo-pentane

: 239482-90-7
N,N'-bis(tert-butyoxycarbonyl)-N''-(4-chlorobenzyl)-N''-(5-pyrrolidin-1-yl-pentyl)-guanidine

Guidance literature:: Multi-step reaction with 4 steps

1.1: NaH / dimethylformamide / 0.5 h / 0 - 20 °C

1.2: dimethylformamide / 18 h / 20 °C

2.1: acetonitrile / 18 h / 20 °C

3.1: HCl / dioxane / 1 h / 20 °C

4.1: NEt₃; Hg(II)Cl₂ / CH₂Cl₂ / 18 h / 0 - 20 °C

With hydrogenchloride; sodium hydride; triethylamine; mercury dichloride; In 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide; acetonitrile; 1.1: deprotonation / 1.2: Alkylation / 2.1: Substitution / 3.1: acidolysis / 4.1: guanylation;
DOI:10.1021/jm990952j

Reference yield:

: 104-86-9
4-chlorobenzylamine

: 239482-90-7
N,N'-bis(tert-butyoxycarbonyl)-N''-(4-chlorobenzyl)-N''-(5-pyrrolidin-1-yl-pentyl)-guanidine

Guidance literature:: Multi-step reaction with 5 steps

1.1: 80 percent / dioxane / 0.75 h / 20 °C

2.1: NaH / dimethylformamide / 0.5 h / 0 - 20 °C

2.2: dimethylformamide / 18 h / 20 °C

3.1: acetonitrile / 18 h / 20 °C

4.1: HCl / dioxane / 1 h / 20 °C

5.1: NEt₃; Hg(II)Cl₂ / CH₂Cl₂ / 18 h / 0 - 20 °C

With hydrogenchloride; sodium hydride; triethylamine; mercury dichloride; In 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide; acetonitrile; 1.1: Acylation / 2.1: deprotonation / 2.2: Alkylation / 3.1: Substitution / 4.1: acidolysis / 5.1: guanylation;
DOI:10.1021/jm990952j