4-(chloromethyl)-6-phenyl-5-tosyl-1,2,3,4-tetrahydropyrimidin-2-one

Base Information

• Chemical Name: 4-(chloromethyl)-6-phenyl-5-tosyl-1,2,3,4-tetrahydropyrimidin-2-one
• CAS No.: 1332329-78-8
• Molecular Formula: C₁₈H₁₇ClN₂O₃S
• Molecular Weight: 376.864
• Mol file: 1332329-78-8.mol

Synonyms:4-(chloromethyl)-6-phenyl-5-tosyl-1,2,3,4-tetrahydropyrimidin-2-one

Chemical Property of 4-(chloromethyl)-6-phenyl-5-tosyl-1,2,3,4-tetrahydropyrimidin-2-one

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 4-(chloromethyl)-6-phenyl-5-tosyl-1,2,3,4-tetrahydropyrimidin-2-one

There total 5 articles about 4-(chloromethyl)-6-phenyl-5-tosyl-1,2,3,4-tetrahydropyrimidin-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:

C36H32N2O4PS(1+)*Cl(1-) → 4-(chloromethyl)-6-phenyl-5-tosyl-1,2,3,4-tetrahydropyrimidin-2-one (1332329-78-8)

Guidance literature:

In acetonitrile; for 0.383333h; Reflux;

DOI:10.1016/j.tet.2011.06.089

Reference yield:

4-(hydroxymethyl)-6-phenyl-5-tosyl-1,2,3,4-tetrahydropyrimidin-2-one (1332329-76-6) → 4-(chloromethyl)-6-phenyl-5-tosyl-1,2,3,4-tetrahydropyrimidin-2-one (1332329-78-8)

Guidance literature:

Multi-step reaction with 2 steps

1: tetrachloromethane / acetonitrile / 20 °C

2: acetonitrile / 0.38 h / Reflux

With tetrachloromethane; In acetonitrile;

DOI:10.1016/j.tet.2011.06.089

Reference yield:

N-[(1-benzoyloxy-4-oxo-4-phenyl-3-tosyl)but-2-yl]urea (1332329-74-4) → 4-(chloromethyl)-6-phenyl-5-tosyl-1,2,3,4-tetrahydropyrimidin-2-one (1332329-78-8)

Guidance literature:

Multi-step reaction with 4 steps

1: toluene-4-sulfonic acid / acetonitrile / 20 h / Reflux

2: water; potassium hydroxide / ethanol / 2 h / 20 °C

3: tetrachloromethane / acetonitrile / 20 °C

4: acetonitrile / 0.38 h / Reflux

With tetrachloromethane; water; toluene-4-sulfonic acid; potassium hydroxide; In ethanol; acetonitrile;

DOI:10.1016/j.tet.2011.06.089

upstream raw materials:

4-(hydroxymethyl)-6-phenyl-5-tosyl-1,2,3,4-tetrahydropyrimidin-2-one

N-[(1-benzoyloxy-4-oxo-4-phenyl-3-tosyl)but-2-yl]urea

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

1-phenyl-2-tosylethanone

Downstream raw materials:

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

4-[di(ethoxycarbonyl)methyl]-7-phenyl-6-tosyl-2,3,4,5-tetrahydro-1H-1,3-diazepin-2-one