1-(2-cyanobenzyl)-3-(4-fluorophenyl)-4-(2-methylsulfinylpyrimidin-4-yl)-4-imidazolin-2-one

Base Information

Chemical Name:1-(2-cyanobenzyl)-3-(4-fluorophenyl)-4-(2-methylsulfinylpyrimidin-4-yl)-4-imidazolin-2-one
CAS No.:521092-13-7
Molecular Formula:C₂₂H₁₆FN₅O₂S
Molecular Weight:433.466
Hs Code.:

Synonyms:1-(2-cyanobenzyl)-3-(4-fluorophenyl)-4-(2-methylsulfinylpyrimidin-4-yl)-4-imidazolin-2-one

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Chemical Property of 1-(2-cyanobenzyl)-3-(4-fluorophenyl)-4-(2-methylsulfinylpyrimidin-4-yl)-4-imidazolin-2-one

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Technology Process of 1-(2-cyanobenzyl)-3-(4-fluorophenyl)-4-(2-methylsulfinylpyrimidin-4-yl)-4-imidazolin-2-one

There total 10 articles about 1-(2-cyanobenzyl)-3-(4-fluorophenyl)-4-(2-methylsulfinylpyrimidin-4-yl)-4-imidazolin-2-one 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:

: 1-(2-cyanobenzyl)-3-(4-fluorophenyl)-4-(2-methylsulfanylpyrimidin-4-yl)-4-imidazolin-2-one

: 521092-13-7
1-(2-cyanobenzyl)-3-(4-fluorophenyl)-4-(2-methylsulfinylpyrimidin-4-yl)-4-imidazolin-2-one

Guidance literature:: 1-(2-cyanobenzyl)-3-(4-fluorophenyl)-4-(2-methylsulfanylpyrimidin-4-yl)-4-imidazolin-2-one; With 3-chloro-benzenecarboperoxoic acid; In chloroform; at 20 ℃; for 1h;

With calcium hydroxide; In chloroform; at 20 ℃; for 2h;

Reference yield:

: 49844-90-8
4-Chloro-2-methylthiopyrimidine

: 521092-13-7
1-(2-cyanobenzyl)-3-(4-fluorophenyl)-4-(2-methylsulfinylpyrimidin-4-yl)-4-imidazolin-2-one

Guidance literature:: Multi-step reaction with 8 steps

1.1: bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide / 3 h / 80 °C

1.2: 20 °C

2.1: hydrogenchloride / water; acetone / 1 h / 20 °C

3.1: hydroxylamine hydrochloride; sodium acetate / methanol / 0.5 h / Heating / reflux

4.1: triethylamine / dichloromethane / 20 °C

5.1: tetrahydrofuran / 0 - 20 °C

5.2: 4 h / 0 - 20 °C

6.1: tetrahydrofuran / 0.5 h / 0 - 20 °C

6.2: 20 °C

7.1: sodium hydride / N,N-dimethyl-formamide / 2 h / 20 °C

8.1: 3-chloro-benzenecarboperoxoic acid / chloroform / 1 h / 20 °C

8.2: 2 h / 20 °C

With hydrogenchloride; hydroxylamine hydrochloride; sodium acetate; sodium hydride; triethylamine; 3-chloro-benzenecarboperoxoic acid; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; methanol; dichloromethane; chloroform; water; N,N-dimethyl-formamide; acetone;

Reference yield:

: 521092-49-9
2,2-dimethoxy-2-(2-methylsulfanylpyrimidin-4-yl)ethylamine

: 521092-13-7
1-(2-cyanobenzyl)-3-(4-fluorophenyl)-4-(2-methylsulfinylpyrimidin-4-yl)-4-imidazolin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: tetrahydrofuran / 0.5 h / 0 - 20 °C

1.2: 20 °C

2.1: sodium hydride / N,N-dimethyl-formamide / 2 h / 20 °C

3.1: 3-chloro-benzenecarboperoxoic acid / chloroform / 1 h / 20 °C

3.2: 2 h / 20 °C

With sodium hydride; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; chloroform; N,N-dimethyl-formamide;