7-phenyl-6-phenylthio-4-succinimido-2,3,4,5-tetrahydro-1H-1,3-diazepin-2-one

Base Information

Chemical Name:7-phenyl-6-phenylthio-4-succinimido-2,3,4,5-tetrahydro-1H-1,3-diazepin-2-one
CAS No.:1353137-54-8
Molecular Formula:C₂₁H₁₉N₃O₃S
Molecular Weight:393.466
Hs Code.:

Synonyms:7-phenyl-6-phenylthio-4-succinimido-2,3,4,5-tetrahydro-1H-1,3-diazepin-2-one

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Chemical Property of 7-phenyl-6-phenylthio-4-succinimido-2,3,4,5-tetrahydro-1H-1,3-diazepin-2-one

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Technology Process of 7-phenyl-6-phenylthio-4-succinimido-2,3,4,5-tetrahydro-1H-1,3-diazepin-2-one

There total 4 articles about 7-phenyl-6-phenylthio-4-succinimido-2,3,4,5-tetrahydro-1H-1,3-diazepin-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: 92.0%

: 123-56-8,89963-74-6
Succinimide

: 1353137-39-9
4-(mesyloxymethyl)-6-phenyl-5-phenylthio-1,2,3,4-tetrahydropyrimidin-2-one

: 1353137-54-8
7-phenyl-6-phenylthio-4-succinimido-2,3,4,5-tetrahydro-1H-1,3-diazepin-2-one

Guidance literature:: Succinimide; With sodium hydride; In tetrahydrofuran; at 20 ℃; for 1h;

4-(mesyloxymethyl)-6-phenyl-5-phenylthio-1,2,3,4-tetrahydropyrimidin-2-one; In tetrahydrofuran; for 4h; Reflux;
DOI:10.1039/c1ob06284k

Reference yield:

: N-[1-benzoyloxy-4-oxo-4-phenyl-3-phenylthiobut-2-yl]urea

: 1353137-54-8
7-phenyl-6-phenylthio-4-succinimido-2,3,4,5-tetrahydro-1H-1,3-diazepin-2-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: toluene-4-sulfonic acid / acetonitrile / 4 h / Reflux

2.1: potassium hydroxide / ethanol; water / 2.83 h / 20 °C

2.2: pH 6

3.1: dmap / dichloromethane / 2 h / 20 °C / Cooling with ice

4.1: sodium hydride / tetrahydrofuran / 1 h / 20 °C

4.2: 4 h / Reflux

With dmap; sodium hydride; toluene-4-sulfonic acid; potassium hydroxide; In tetrahydrofuran; ethanol; dichloromethane; water; acetonitrile;
DOI:10.1039/c1ob06284k

Reference yield:

: 4-(benzoyloxymethyl)-6-phenyl-5-phenylthio-1,2,3,4-tetrahydropyrimidin-2-one

: 1353137-54-8
7-phenyl-6-phenylthio-4-succinimido-2,3,4,5-tetrahydro-1H-1,3-diazepin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium hydroxide / ethanol; water / 2.83 h / 20 °C

1.2: pH 6

2.1: dmap / dichloromethane / 2 h / 20 °C / Cooling with ice

3.1: sodium hydride / tetrahydrofuran / 1 h / 20 °C

3.2: 4 h / Reflux

With dmap; sodium hydride; potassium hydroxide; In tetrahydrofuran; ethanol; dichloromethane; water;
DOI:10.1039/c1ob06284k