4,4'-(2,4,6-trimethyl-1,4-dihydropyridine-3,5-diyl)bis(6-(4-chlorophenyl)-5,6-di-hydropyrimidine-2(1H)-thione)

Base Information

• Chemical Name: 4,4'-(2,4,6-trimethyl-1,4-dihydropyridine-3,5-diyl)bis(6-(4-chlorophenyl)-5,6-di-hydropyrimidine-2(1H)-thione)
• CAS No.: 1447968-02-6
• Molecular Formula: C₂₈H₂₇Cl₂N₅S₂
• Molecular Weight: 568.594

Synonyms:4,4'-(2,4,6-trimethyl-1,4-dihydropyridine-3,5-diyl)bis(6-(4-chlorophenyl)-5,6-di-hydropyrimidine-2(1H)-thione)

Chemical Property of 4,4'-(2,4,6-trimethyl-1,4-dihydropyridine-3,5-diyl)bis(6-(4-chlorophenyl)-5,6-di-hydropyrimidine-2(1H)-thione)

Chemical Property:

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Technology Process of 4,4'-(2,4,6-trimethyl-1,4-dihydropyridine-3,5-diyl)bis(6-(4-chlorophenyl)-5,6-di-hydropyrimidine-2(1H)-thione)

There total 3 articles about 4,4'-(2,4,6-trimethyl-1,4-dihydropyridine-3,5-diyl)bis(6-(4-chlorophenyl)-5,6-di-hydropyrimidine-2(1H)-thione) 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: 60.0%

(2E,2'E)-1,1'-(2,4,6-trimethyl-1,4-dihydropyridine-3,5-diyl)bis(3-(4-chlorophenyl)prop-2-en-1-one) (1447967-99-8) + thiourea (17356-08-0) → 4,4'-(2,4,6-trimethyl-1,4-dihydropyridine-3,5-diyl)bis(6-(4-chlorophenyl)-5,6-di-hydropyrimidine-2(1H)-thione) (1447968-02-6)

Guidance literature:

With sodium ethanolate; for 4h; Reflux;

DOI:10.1016/j.saa.2012.12.069

Reference yield:

3,5-diacetyl-1,4-dihydro-2,4,6-trimethylpyridine (1081-09-0) → 4,4'-(2,4,6-trimethyl-1,4-dihydropyridine-3,5-diyl)bis(6-(4-chlorophenyl)-5,6-di-hydropyrimidine-2(1H)-thione) (1447968-02-6)

Guidance literature:

Multi-step reaction with 2 steps

1: potassium hydroxide / 20 °C

2: sodium ethanolate / 4 h / Reflux

With sodium ethanolate; potassium hydroxide;

DOI:10.1016/j.saa.2012.12.069

Reference yield:

4-chlorobenzaldehyde (104-88-1) → 4,4'-(2,4,6-trimethyl-1,4-dihydropyridine-3,5-diyl)bis(6-(4-chlorophenyl)-5,6-di-hydropyrimidine-2(1H)-thione) (1447968-02-6)

Guidance literature:

Multi-step reaction with 2 steps

1: potassium hydroxide / 20 °C

2: sodium ethanolate / 4 h / Reflux

With sodium ethanolate; potassium hydroxide;

DOI:10.1016/j.saa.2012.12.069

upstream raw materials:

(2E,2'E)-1,1'-(2,4,6-trimethyl-1,4-dihydropyridine-3,5-diyl)bis(3-(4-chlorophenyl)prop-2-en-1-one)

thiourea

3,5-diacetyl-1,4-dihydro-2,4,6-trimethylpyridine

4-chlorobenzaldehyde

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