ethyl ({({7-[amino(imino)methyl]-2-naphthyl}methyl)[4-(4-ethanimidoyl-1,4-diazepan-1-yl)phenyl]amino}sulfonyl)acetate

Base Information

Chemical Name:ethyl ({({7-[amino(imino)methyl]-2-naphthyl}methyl)[4-(4-ethanimidoyl-1,4-diazepan-1-yl)phenyl]amino}sulfonyl)acetate
CAS No.:220220-41-7
Molecular Formula:C₂₉H₃₆N₆O₄S
Molecular Weight:564.709
Hs Code.:

Synonyms:ethyl ({({7-[amino(imino)methyl]-2-naphthyl}methyl)[4-(4-ethanimidoyl-1,4-diazepan-1-yl)phenyl]amino}sulfonyl)acetate

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Chemical Property of ethyl ({({7-[amino(imino)methyl]-2-naphthyl}methyl)[4-(4-ethanimidoyl-1,4-diazepan-1-yl)phenyl]amino}sulfonyl)acetate

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Technology Process of ethyl ({({7-[amino(imino)methyl]-2-naphthyl}methyl)[4-(4-ethanimidoyl-1,4-diazepan-1-yl)phenyl]amino}sulfonyl)acetate

There total 6 articles about ethyl ({({7-[amino(imino)methyl]-2-naphthyl}methyl)[4-(4-ethanimidoyl-1,4-diazepan-1-yl)phenyl]amino}sulfonyl)acetate 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: 17.0%

: 2208-07-3
ethyl acetimidate hydrochloride

: 286430-94-2
ethyl ({({7-[amino(imino)methyl]-2-naphthyl}methyl)[4-(1,4-diazepan-1-yl)phenyl]amino}sulfonyl)acetate

: 220220-41-7
ethyl ({({7-[amino(imino)methyl]-2-naphthyl}methyl)[4-(4-ethanimidoyl-1,4-diazepan-1-yl)phenyl]amino}sulfonyl)acetate

Guidance literature:: With triethylamine; In ethanol; at 20 ℃; for 24h;
DOI:10.1016/j.bmc.2004.02.022

Reference yield:

: 350-46-9,178603-76-4
4-Fluoronitrobenzene

: 220220-41-7
ethyl ({({7-[amino(imino)methyl]-2-naphthyl}methyl)[4-(4-ethanimidoyl-1,4-diazepan-1-yl)phenyl]amino}sulfonyl)acetate

Guidance literature:: Multi-step reaction with 6 steps

1.1: 83 percent / potassium carbonate / dimethylformamide / 13 h / 90 °C

2.1: H₂ / Pd/C / ethanol / 16 h / 20 °C

3.1: 15.8 g / acetic acid; sodium triacetoxyborohydride / 1,2-dichloro-ethane / 5 h

4.1: 87 percent / pyridine / 1,2-dichloro-ethane / 12 h / 20 °C

5.1: hydrogen chloride; ethanol / 15 h / 5 °C

5.2: 99 percent / ammonium acetate / ethanol / 24 h / 20 °C

6.1: 17 percent / triethylamine / ethanol / 24 h / 20 °C

With pyridine; hydrogenchloride; ethanol; hydrogen; sodium tris(acetoxy)borohydride; potassium carbonate; acetic acid; triethylamine; palladium on activated charcoal; In ethanol; 1,2-dichloro-ethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2004.02.022

Reference yield:

: 220220-23-5
tert-butyl 4-(4-nitrophenyl)-1,4-diazepane-1-carboxylate

: 220220-41-7
ethyl ({({7-[amino(imino)methyl]-2-naphthyl}methyl)[4-(4-ethanimidoyl-1,4-diazepan-1-yl)phenyl]amino}sulfonyl)acetate

Guidance literature:: Multi-step reaction with 5 steps

1.1: H₂ / Pd/C / ethanol / 16 h / 20 °C

2.1: 15.8 g / acetic acid; sodium triacetoxyborohydride / 1,2-dichloro-ethane / 5 h

3.1: 87 percent / pyridine / 1,2-dichloro-ethane / 12 h / 20 °C

4.1: hydrogen chloride; ethanol / 15 h / 5 °C

4.2: 99 percent / ammonium acetate / ethanol / 24 h / 20 °C

5.1: 17 percent / triethylamine / ethanol / 24 h / 20 °C

With pyridine; hydrogenchloride; ethanol; hydrogen; sodium tris(acetoxy)borohydride; acetic acid; triethylamine; palladium on activated charcoal; In ethanol; 1,2-dichloro-ethane;
DOI:10.1016/j.bmc.2004.02.022