(Z)-3-((hydroxy(2-(2-((4-oxo-3-phenyl-4,5-dihydro-3H-pyrimido[5,4-b]indol-2-yl)thio)acetamido)ethoxy)phosphoryl)oxy)propane-1,2-diyl dioleate

Base Information

Chemical Name:(Z)-3-((hydroxy(2-(2-((4-oxo-3-phenyl-4,5-dihydro-3H-pyrimido[5,4-b]indol-2-yl)thio)acetamido)ethoxy)phosphoryl)oxy)propane-1,2-diyl dioleate
CAS No.:1438280-68-2
Molecular Formula:C₅₉H₈₉N₄O₁₀PS
Molecular Weight:1077.42
Hs Code.:

Synonyms:(Z)-3-((hydroxy(2-(2-((4-oxo-3-phenyl-4,5-dihydro-3H-pyrimido[5,4-b]indol-2-yl)thio)acetamido)ethoxy)phosphoryl)oxy)propane-1,2-diyl dioleate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (Z)-3-((hydroxy(2-(2-((4-oxo-3-phenyl-4,5-dihydro-3H-pyrimido[5,4-b]indol-2-yl)thio)acetamido)ethoxy)phosphoryl)oxy)propane-1,2-diyl dioleate

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Technology Process of (Z)-3-((hydroxy(2-(2-((4-oxo-3-phenyl-4,5-dihydro-3H-pyrimido[5,4-b]indol-2-yl)thio)acetamido)ethoxy)phosphoryl)oxy)propane-1,2-diyl dioleate

There total 6 articles about (Z)-3-((hydroxy(2-(2-((4-oxo-3-phenyl-4,5-dihydro-3H-pyrimido[5,4-b]indol-2-yl)thio)acetamido)ethoxy)phosphoryl)oxy)propane-1,2-diyl dioleate 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: 10.9%

: 2462-63-7,4004-05-1,5683-50-1,5683-54-5,7768-07-2,16777-83-6,16810-06-3,19805-18-6
dioleoylphosphatidylethanolamine

: 1438280-85-3
(2-((4-oxo-3-phenyl-4,5-dihydro-3H-pyrimido[5,4-b]indol-2-yl)thio)acetic acid)

: 1438280-68-2
(Z)-3-((hydroxy(2-(2-((4-oxo-3-phenyl-4,5-dihydro-3H-pyrimido[5,4-b]indol-2-yl)thio)acetamido)ethoxy)phosphoryl)oxy)propane-1,2-diyl dioleate

Guidance literature:: With triethylamine; HATU; In N,N-dimethyl-formamide; at 22 - 24 ℃;
DOI:10.1021/jm301694x

Reference yield:

: 1885-29-6
anthranilic acid nitrile

: 1438280-68-2
(Z)-3-((hydroxy(2-(2-((4-oxo-3-phenyl-4,5-dihydro-3H-pyrimido[5,4-b]indol-2-yl)thio)acetamido)ethoxy)phosphoryl)oxy)propane-1,2-diyl dioleate

Guidance literature:: Multi-step reaction with 6 steps

1: sodium hydrogencarbonate / ethanol / 42 h / Reflux

2: potassium tert-butylate / tetrahydrofuran / 2.75 h / 30 °C / Inert atmosphere

3: ethanol / 6 h / Reflux

4: acetyl chloride / ethanol / 12 h / Inert atmosphere; Reflux

5: potassium hydroxide / ethanol / 6 h / Reflux

6: HATU; triethylamine / N,N-dimethyl-formamide / 22 - 24 °C

With potassium tert-butylate; sodium hydrogencarbonate; triethylamine; acetyl chloride; HATU; potassium hydroxide; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide;
DOI:10.1021/jm301694x

Reference yield:

: 87223-76-5
(2-cyanophenylamino)acetic acid ethyl ester

: 1438280-68-2
(Z)-3-((hydroxy(2-(2-((4-oxo-3-phenyl-4,5-dihydro-3H-pyrimido[5,4-b]indol-2-yl)thio)acetamido)ethoxy)phosphoryl)oxy)propane-1,2-diyl dioleate

Guidance literature:: Multi-step reaction with 5 steps

1: potassium tert-butylate / tetrahydrofuran / 2.75 h / 30 °C / Inert atmosphere

2: ethanol / 6 h / Reflux

3: acetyl chloride / ethanol / 12 h / Inert atmosphere; Reflux

4: potassium hydroxide / ethanol / 6 h / Reflux

5: HATU; triethylamine / N,N-dimethyl-formamide / 22 - 24 °C

With potassium tert-butylate; triethylamine; acetyl chloride; HATU; potassium hydroxide; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide;
DOI:10.1021/jm301694x