2-(4-((2-(2-nitrophenyl)propyl)amino)-2-oxopyrimidin-1(2H)-yl)acetic acid

Base Information

Chemical Name:2-(4-((2-(2-nitrophenyl)propyl)amino)-2-oxopyrimidin-1(2H)-yl)acetic acid
CAS No.:1443322-84-6
Molecular Formula:C₁₅H₁₆N₄O₅
Molecular Weight:332.316
Hs Code.:

Synonyms:2-(4-((2-(2-nitrophenyl)propyl)amino)-2-oxopyrimidin-1(2H)-yl)acetic acid

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Chemical Property of 2-(4-((2-(2-nitrophenyl)propyl)amino)-2-oxopyrimidin-1(2H)-yl)acetic acid

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Technology Process of 2-(4-((2-(2-nitrophenyl)propyl)amino)-2-oxopyrimidin-1(2H)-yl)acetic acid

There total 3 articles about 2-(4-((2-(2-nitrophenyl)propyl)amino)-2-oxopyrimidin-1(2H)-yl)acetic 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: 95.0%

: 1443322-79-9
tert-butyl 2-(4-((2-(2-nitrophenyl)propyl)amino)-2-oxopyrimidin-1(2H)-yl)acetate

: 1443322-84-6
2-(4-((2-(2-nitrophenyl)propyl)amino)-2-oxopyrimidin-1(2H)-yl)acetic acid

Guidance literature:: With trifluoroacetic acid; at 20 ℃; for 1h;
DOI:10.1002/psc.2514

Reference yield:

: C₁₀H₁₃ClN₂O₃

: 1443322-84-6
2-(4-((2-(2-nitrophenyl)propyl)amino)-2-oxopyrimidin-1(2H)-yl)acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine; lithium chloride / dichloromethane / 20 h / 0 - 20 °C

2: trifluoroacetic acid / 1 h / 20 °C

With triethylamine; trifluoroacetic acid; lithium chloride; In dichloromethane;
DOI:10.1002/psc.2514

Reference yield:

: 257869-92-4
tert-butyl uracil-1-ylacetate

: 1443322-84-6
2-(4-((2-(2-nitrophenyl)propyl)amino)-2-oxopyrimidin-1(2H)-yl)acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine; dmap; 2-mesitylenesulphonyl chloride / dichloromethane / 6 h / 20 °C / Inert atmosphere

2: triethylamine; lithium chloride / dichloromethane / 20 h / 0 - 20 °C

3: trifluoroacetic acid / 1 h / 20 °C

With dmap; 2-mesitylenesulphonyl chloride; triethylamine; trifluoroacetic acid; lithium chloride; In dichloromethane;
DOI:10.1002/psc.2514