(E)-methyl 3-(4-(2-((E)-3-(3-(7-chloroquinolin-4-ylamino)propyl)-2-phenylguanidino)phenoxy)phenyl)-2-methylacrylate

Base Information

Chemical Name:(E)-methyl 3-(4-(2-((E)-3-(3-(7-chloroquinolin-4-ylamino)propyl)-2-phenylguanidino)phenoxy)phenyl)-2-methylacrylate
CAS No.:1596272-45-5
Molecular Formula:C₃₆H₃₄ClN₅O₃
Molecular Weight:620.151
Hs Code.:

Synonyms:(E)-methyl 3-(4-(2-((E)-3-(3-(7-chloroquinolin-4-ylamino)propyl)-2-phenylguanidino)phenoxy)phenyl)-2-methylacrylate

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Chemical Property of (E)-methyl 3-(4-(2-((E)-3-(3-(7-chloroquinolin-4-ylamino)propyl)-2-phenylguanidino)phenoxy)phenyl)-2-methylacrylate

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Technology Process of (E)-methyl 3-(4-(2-((E)-3-(3-(7-chloroquinolin-4-ylamino)propyl)-2-phenylguanidino)phenoxy)phenyl)-2-methylacrylate

There total 8 articles about (E)-methyl 3-(4-(2-((E)-3-(3-(7-chloroquinolin-4-ylamino)propyl)-2-phenylguanidino)phenoxy)phenyl)-2-methylacrylate 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: 70.0%

: 7597-14-0
N-(7-chloroquinolin-4-yl)propane-1,3-diamine

: 1596272-32-0
(E)-methyl 2-methyl-3-(4-(2-(3-phenylthioureido)phenoxy)phenyl)acrylate

: 1596272-45-5
(E)-methyl 3-(4-(2-((E)-3-(3-(7-chloroquinolin-4-ylamino)propyl)-2-phenylguanidino)phenoxy)phenyl)-2-methylacrylate

Guidance literature:: With triethylamine; mercury dichloride; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1016/j.bmcl.2014.02.044

Reference yield:

: 123-08-0,65581-83-1
4-hydroxy-benzaldehyde

: 1596272-45-5
(E)-methyl 3-(4-(2-((E)-3-(3-(7-chloroquinolin-4-ylamino)propyl)-2-phenylguanidino)phenoxy)phenyl)-2-methylacrylate

Guidance literature:: Multi-step reaction with 7 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 3 h / 20 °C

2.1: 1,4-diaza-bicyclo[2.2.2]octane / neat (no solvent) / 0.33 h / 20 °C

2.2: 255 / 72 h / 20 °C

3.1: pyridine / dichloromethane / 0.5 h / 0 - 20 °C

4.1: sodium tetrahydroborate / methanol / 0.83 h / 0 - 20 °C

5.1: iron; acetic acid / 0.33 h / 90 °C

6.1: N,N-dimethyl-formamide / 20 °C

7.1: triethylamine; mercury dichloride / N,N-dimethyl-formamide / 20 °C

With pyridine; 1,4-diaza-bicyclo[2.2.2]octane; sodium tetrahydroborate; iron; potassium carbonate; acetic acid; triethylamine; mercury dichloride; In methanol; dichloromethane; N,N-dimethyl-formamide; 2.1: |Morita-Baylis-Hillman Alkylation / 2.2: |Morita-Baylis-Hillman Alkylation;
DOI:10.1016/j.bmcl.2014.02.044

Reference yield:

: 1493-27-2,127723-77-7
ortho-nitrofluorobenzene

: 1596272-45-5
(E)-methyl 3-(4-(2-((E)-3-(3-(7-chloroquinolin-4-ylamino)propyl)-2-phenylguanidino)phenoxy)phenyl)-2-methylacrylate

Guidance literature:: Multi-step reaction with 7 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 3 h / 20 °C

2.1: 1,4-diaza-bicyclo[2.2.2]octane / neat (no solvent) / 0.33 h / 20 °C

2.2: 255 / 72 h / 20 °C

3.1: pyridine / dichloromethane / 0.5 h / 0 - 20 °C

4.1: sodium tetrahydroborate / methanol / 0.83 h / 0 - 20 °C

5.1: iron; acetic acid / 0.33 h / 90 °C

6.1: N,N-dimethyl-formamide / 20 °C

7.1: triethylamine; mercury dichloride / N,N-dimethyl-formamide / 20 °C

With pyridine; 1,4-diaza-bicyclo[2.2.2]octane; sodium tetrahydroborate; iron; potassium carbonate; acetic acid; triethylamine; mercury dichloride; In methanol; dichloromethane; N,N-dimethyl-formamide; 2.1: |Morita-Baylis-Hillman Alkylation / 2.2: |Morita-Baylis-Hillman Alkylation;
DOI:10.1016/j.bmcl.2014.02.044