(S)-N-(1-(2-((4-amino-3-nitrophenyl)amino)-6-propylpyrimidin-4-yl)pyrrolidin-3-yl)acetamide

Base Information

Chemical Name:(S)-N-(1-(2-((4-amino-3-nitrophenyl)amino)-6-propylpyrimidin-4-yl)pyrrolidin-3-yl)acetamide
CAS No.:1394316-91-6
Molecular Formula:C₁₉H₂₅N₇O₃
Molecular Weight:399.453
Hs Code.:

Synonyms:(S)-N-(1-(2-((4-amino-3-nitrophenyl)amino)-6-propylpyrimidin-4-yl)pyrrolidin-3-yl)acetamide

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Chemical Property of (S)-N-(1-(2-((4-amino-3-nitrophenyl)amino)-6-propylpyrimidin-4-yl)pyrrolidin-3-yl)acetamide

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Technology Process of (S)-N-(1-(2-((4-amino-3-nitrophenyl)amino)-6-propylpyrimidin-4-yl)pyrrolidin-3-yl)acetamide

There total 5 articles about (S)-N-(1-(2-((4-amino-3-nitrophenyl)amino)-6-propylpyrimidin-4-yl)pyrrolidin-3-yl)acetamide 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: 86.0%

: 114636-37-2
tert-butyl (3S)-3-acetamidopyrrolidine-1-carboxylate

: 2-((4-amino-3-nitrophenyl)amino)-6-propylpyrimidin-4-yl 4-methylbenzenesulfonate

: 1394316-91-6
(S)-N-(1-(2-((4-amino-3-nitrophenyl)amino)-6-propylpyrimidin-4-yl)pyrrolidin-3-yl)acetamide

Guidance literature:: tert-butyl (3S)-3-acetamidopyrrolidine-1-carboxylate; With toluene-4-sulfonic acid; In toluene; at 20 ℃; for 6h;

2-((4-amino-3-nitrophenyl)amino)-6-propylpyrimidin-4-yl 4-methylbenzenesulfonate; With N-ethyl-N,N-diisopropylamine; In toluene; at 80 - 90 ℃; for 5h;

Reference yield:

: 5307-14-2,183870-67-9
2-nitro-1,4-phenylenediamine

: 1394316-91-6
(S)-N-(1-(2-((4-amino-3-nitrophenyl)amino)-6-propylpyrimidin-4-yl)pyrrolidin-3-yl)acetamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: (S)-N-(1-(2-((4-amino-3-nitrophenyl)amino)-6-propylpyrimidin-4-yl)pyrrolidin-3-yl)acetamide hydrochloride / water / 3 h / 80 - 90 °C

1.2: 2 h / 65 °C

2.1: butan-1-ol / 15 h / 95 °C

3.1: triethylamine / acetone / 3 h / 20 °C

4.1: toluene-4-sulfonic acid / toluene / 6 h / 20 °C

4.2: 5 h / 80 - 90 °C

With (S)-N-(1-(2-((4-amino-3-nitrophenyl)amino)-6-propylpyrimidin-4-yl)pyrrolidin-3-yl)acetamide hydrochloride; toluene-4-sulfonic acid; triethylamine; In water; acetone; toluene; butan-1-ol;

Reference yield:

: 1-(4-amino-3-nitrophenyl)guanidine hemicarbonate

: 1394316-91-6
(S)-N-(1-(2-((4-amino-3-nitrophenyl)amino)-6-propylpyrimidin-4-yl)pyrrolidin-3-yl)acetamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: butan-1-ol / 15 h / 95 °C

2.1: triethylamine / acetone / 3 h / 20 °C

3.1: toluene-4-sulfonic acid / toluene / 6 h / 20 °C

3.2: 5 h / 80 - 90 °C

With toluene-4-sulfonic acid; triethylamine; In acetone; toluene; butan-1-ol;