(R)-((3-(5-(2,5-dichloro-4-((4-(4-cyclopropyl-1,2,3,4-tetrahydroquinoxaline-1-carbonyl)thiazolidin-3-yl)methyl)phenyl)pentyl)ureido)methyl)phosphonic acid

Base Information

Chemical Name:(R)-((3-(5-(2,5-dichloro-4-((4-(4-cyclopropyl-1,2,3,4-tetrahydroquinoxaline-1-carbonyl)thiazolidin-3-yl)methyl)phenyl)pentyl)ureido)methyl)phosphonic acid
CAS No.:1445984-64-4
Molecular Formula:C₂₉H₃₈Cl₂N₅O₅PS
Molecular Weight:670.597
Hs Code.:

(R)-((3-(5-(2,5-dichloro-4-((4-(4-cyclopropyl-1,2,3,4-tetrahydroquinoxaline-1-carbonyl)thiazolidin-3-yl)methyl)phenyl)pentyl)ureido)methyl)phosphonic acid

Synonyms:

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Chemical Property of (R)-((3-(5-(2,5-dichloro-4-((4-(4-cyclopropyl-1,2,3,4-tetrahydroquinoxaline-1-carbonyl)thiazolidin-3-yl)methyl)phenyl)pentyl)ureido)methyl)phosphonic acid

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Technology Process of (R)-((3-(5-(2,5-dichloro-4-((4-(4-cyclopropyl-1,2,3,4-tetrahydroquinoxaline-1-carbonyl)thiazolidin-3-yl)methyl)phenyl)pentyl)ureido)methyl)phosphonic acid

There total 12 articles about (R)-((3-(5-(2,5-dichloro-4-((4-(4-cyclopropyl-1,2,3,4-tetrahydroquinoxaline-1-carbonyl)thiazolidin-3-yl)methyl)phenyl)pentyl)ureido)methyl)phosphonic acid 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:

: C₃₃H₄₆Cl₂N₅O₅PS

: 1445984-64-4
(R)-((3-(5-(2,5-dichloro-4-((4-(4-cyclopropyl-1,2,3,4-tetrahydroquinoxaline-1-carbonyl)thiazolidin-3-yl)methyl)phenyl)pentyl)ureido)methyl)phosphonic acid

Guidance literature:: With trimethylsilyl bromide; In N,N-dimethyl-formamide; at 20 ℃; for 3h;
DOI:10.1021/acs.jmedchem.8b00308

Reference yield:

: 1445985-48-7
1-cyclopropyl-4-[[(4R)-1,3-thiazolidin-4-yl]carbonyl]-1,2,3,4-tetrahydroquinoxaline

: 1445984-64-4
(R)-((3-(5-(2,5-dichloro-4-((4-(4-cyclopropyl-1,2,3,4-tetrahydroquinoxaline-1-carbonyl)thiazolidin-3-yl)methyl)phenyl)pentyl)ureido)methyl)phosphonic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate / N,N-dimethyl-formamide

2.1: hydrogenchloride / water; 1,4-dioxane / 1 h

3.1: triethylamine / N,N-dimethyl-formamide / 1 h / 20 °C

3.2: 20 °C

4.1: trimethylsilyl bromide / N,N-dimethyl-formamide / 3 h / 20 °C

With hydrogenchloride; trimethylsilyl bromide; potassium carbonate; triethylamine; In 1,4-dioxane; water; N,N-dimethyl-formamide;
DOI:10.1021/acs.jmedchem.8b00308

Reference yield:

: 381229-84-1
2,5-dichloro-4-formylphenyl trilluoromethanesulfonate

: 1445984-64-4
(R)-((3-(5-(2,5-dichloro-4-((4-(4-cyclopropyl-1,2,3,4-tetrahydroquinoxaline-1-carbonyl)thiazolidin-3-yl)methyl)phenyl)pentyl)ureido)methyl)phosphonic acid

Guidance literature:: Multi-step reaction with 8 steps

1.1: N-ethyl-N,N-diisopropylamine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide / N,N-dimethyl-formamide

2.1: hydrogen; rhodium contaminated with carbon / ethyl acetate

3.1: sodium tetrahydroborate / methanol / 1.5 h / 0 °C

4.1: triphenylphosphine; N-Bromosuccinimide / dichloromethane; tetrahydrofuran / 1 h / 0 - 20 °C

5.1: potassium carbonate / N,N-dimethyl-formamide

6.1: hydrogenchloride / water; 1,4-dioxane / 1 h

7.1: triethylamine / N,N-dimethyl-formamide / 1 h / 20 °C

7.2: 20 °C

8.1: trimethylsilyl bromide / N,N-dimethyl-formamide / 3 h / 20 °C

With hydrogenchloride; bis-triphenylphosphine-palladium(II) chloride; sodium tetrahydroborate; N-Bromosuccinimide; copper(l) iodide; trimethylsilyl bromide; rhodium contaminated with carbon; hydrogen; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; triphenylphosphine; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide; 1.1: |Sonogashira Cross-Coupling;
DOI:10.1021/acs.jmedchem.8b00308