N-(3-chloro-4-methylphenyl)-6-methyl-2-oxo-4-(thiophen-2-yl)-1,2,3,4-tetrahydropyrimidine-5-carboxamide

Base Information

• Chemical Name: N-(3-chloro-4-methylphenyl)-6-methyl-2-oxo-4-(thiophen-2-yl)-1,2,3,4-tetrahydropyrimidine-5-carboxamide
• CAS No.: 5864-00-6
• Molecular Formula: C₁₂H₁₀O₆
• Molecular Weight: 250.208
• DSSTox Substance ID: DTXSID50974181
• Mol file: 5864-00-6.mol

Synonyms:405156-83-4;N-(3-chloro-4-methylphenyl)-6-methyl-2-oxo-4-(thiophen-2-yl)-1,2,3,4-tetrahydropyrimidine-5-carboxamide;CBMicro_035789;DTXSID50974181;AKOS001650882;AKOS021997657;N-(3-chloro-4-methylphenyl)-6-methyl-2-oxo-4-thiophen-2-yl-3,4-dihydro-1H-pyrimidine-5-carboxamide;BIM-0035739.P001;AB00673015-01;SR-01000486521;SR-01000486521-1;F1011-1294;N-(3-Chloro-4-methylphenyl)-2-hydroxy-4-methyl-6-(thiophen-2-yl)-1,6-dihydropyrimidine-5-carboximidic acid

Chemical Property of N-(3-chloro-4-methylphenyl)-6-methyl-2-oxo-4-(thiophen-2-yl)-1,2,3,4-tetrahydropyrimidine-5-carboxamide

Chemical Property:

• Vapor Pressure: 1.28E-12mmHg at 25°C
• Boiling Point: 561.1°C at 760 mmHg
• Flash Point: 293.1°C
• PSA: 107.97000
• Density: 1.366g/cm³
• LogP: 1.13970
• XLogP3: 2.7
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 361.0651756
• Heavy Atom Count: 24
• Complexity: 554

Purity/Quality:

97% ^*data from raw suppliers

(5,7-Dihydroxy-4-methyl-2-oxo-2H-chromen-3-yl)-acetic acid ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=C(C=C(C=C1)NC(=O)C2=C(NC(=O)NC2C3=CC=CS3)C)Cl

Technology Process of N-(3-chloro-4-methylphenyl)-6-methyl-2-oxo-4-(thiophen-2-yl)-1,2,3,4-tetrahydropyrimidine-5-carboxamide

There total 6 articles about N-(3-chloro-4-methylphenyl)-6-methyl-2-oxo-4-(thiophen-2-yl)-1,2,3,4-tetrahydropyrimidine-5-carboxamide 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: 78.0%

methyl (5,7-dihydroxy-4-methyl-2-oxochromen-3-yl)acetate (892559-73-8) → (5,7-dihydroxy-4-methyl-2-oxochromen-3-yl)acetic acid (5864-00-6)

Guidance literature:

With sodium hydroxide; In water; isopropyl alcohol; Heating;

DOI:10.1007/s10600-007-0053-x

Reference yield: 25.6%

(5,7-dihydroxy-4-methyl-2-oxo-2H-chromen-3-yl)-acetic acid ethyl ester (5852-00-6) → (5,7-dihydroxy-4-methyl-2-oxochromen-3-yl)acetic acid (5864-00-6)

Guidance literature:

With potassium carbonate; In ethanol; water; for 3h; Reflux;

Reference yield:

3,5-dihydroxyphenol (108-73-6) → (5,7-dihydroxy-4-methyl-2-oxochromen-3-yl)acetic acid (5864-00-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 86 percent / HCl / methanol / 0 - 20 °C

2: 78 percent / NaOH / propan-2-ol; H₂O / 1 h / Heating

With hydrogenchloride; sodium hydroxide; In methanol; water; isopropyl alcohol; 1: Pechmann condensation;

DOI:10.1007/s10600-007-0055-8

upstream raw materials:

3,5-dihydroxyphenol

diethyl acetylsuccinate

(5,7-dihydroxy-4-methyl-2-oxo-2H-chromen-3-yl)-acetic acid ethyl ester

methyl (5,7-dihydroxy-4-methyl-2-oxochromen-3-yl)acetate