(4-(2-(2-aminoethylthio)-3-(3-(4-(3-amino-5-(trifluoromethyl)phenoxy)phenyl)ureido)-5-(trifluoromethyl)phenylcarbamoyl)butyl)guanidine

Base Information

Chemical Name:(4-(2-(2-aminoethylthio)-3-(3-(4-(3-amino-5-(trifluoromethyl)phenoxy)phenyl)ureido)-5-(trifluoromethyl)phenylcarbamoyl)butyl)guanidine
CAS No.:1613588-56-9
Molecular Formula:C₂₉H₃₂F₆N₈O₃S
Molecular Weight:686.681
Hs Code.:

Synonyms:(4-(2-(2-aminoethylthio)-3-(3-(4-(3-amino-5-(trifluoromethyl)phenoxy)phenyl)ureido)-5-(trifluoromethyl)phenylcarbamoyl)butyl)guanidine

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Chemical Property of (4-(2-(2-aminoethylthio)-3-(3-(4-(3-amino-5-(trifluoromethyl)phenoxy)phenyl)ureido)-5-(trifluoromethyl)phenylcarbamoyl)butyl)guanidine

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Technology Process of (4-(2-(2-aminoethylthio)-3-(3-(4-(3-amino-5-(trifluoromethyl)phenoxy)phenyl)ureido)-5-(trifluoromethyl)phenylcarbamoyl)butyl)guanidine

There total 5 articles about (4-(2-(2-aminoethylthio)-3-(3-(4-(3-amino-5-(trifluoromethyl)phenoxy)phenyl)ureido)-5-(trifluoromethyl)phenylcarbamoyl)butyl)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:

: 1613588-51-4
C₃₉H₄₈F₆N₈O₇S

: 1613588-56-9
(4-(2-(2-aminoethylthio)-3-(3-(4-(3-amino-5-(trifluoromethyl)phenoxy)phenyl)ureido)-5-(trifluoromethyl)phenylcarbamoyl)butyl)guanidine

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 1h;

Reference yield:

: 1613588-48-9
4-(3-(trifluoromethyl)-5-nitrophenoxy)benzenamine

: 1613588-56-9
(4-(2-(2-aminoethylthio)-3-(3-(4-(3-amino-5-(trifluoromethyl)phenoxy)phenyl)ureido)-5-(trifluoromethyl)phenylcarbamoyl)butyl)guanidine

Guidance literature:: Multi-step reaction with 3 steps

1.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 0 - 20 °C

1.2: 4 h

2.1: zinc; ammonium chloride / methanol / 20 h / 20 °C

3.1: trifluoroacetic acid / dichloromethane / 1 h / 20 °C

With ammonium chloride; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; zinc; In methanol; dichloromethane;

Reference yield:

: 123-30-8
4-amino-phenol

: 1613588-56-9
(4-(2-(2-aminoethylthio)-3-(3-(4-(3-amino-5-(trifluoromethyl)phenoxy)phenyl)ureido)-5-(trifluoromethyl)phenylcarbamoyl)butyl)guanidine

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 48 h / 110 - 120 °C

2.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 0 - 20 °C

2.2: 4 h

3.1: zinc; ammonium chloride / methanol / 20 h / 20 °C

4.1: trifluoroacetic acid / dichloromethane / 1 h / 20 °C

With potassium carbonate; ammonium chloride; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; zinc; In methanol; dichloromethane; N,N-dimethyl-formamide;