ethyl 2-({[(5-{[(4-methylphenyl)amino]carbonyl}-2-{2-[(4-methylphenyl)amino]-2-oxoethyl}pyrimidin-4-yl)thio]acetyl}amino)-4,5,6,7-tetrahydro-1-benzo[b]thiophene-3-carboxylate

Base Information

• Chemical Name: ethyl 2-({[(5-{[(4-methylphenyl)amino]carbonyl}-2-{2-[(4-methylphenyl)amino]-2-oxoethyl}pyrimidin-4-yl)thio]acetyl}amino)-4,5,6,7-tetrahydro-1-benzo[b]thiophene-3-carboxylate
• CAS No.: 1447585-64-9
• Molecular Formula: C₃₄H₃₅N₅O₅S₂
• Molecular Weight: 657.814

Synonyms:

Chemical Property of ethyl 2-({[(5-{[(4-methylphenyl)amino]carbonyl}-2-{2-[(4-methylphenyl)amino]-2-oxoethyl}pyrimidin-4-yl)thio]acetyl}amino)-4,5,6,7-tetrahydro-1-benzo[b]thiophene-3-carboxylate

Chemical Property:

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Useful:

Technology Process of ethyl 2-({[(5-{[(4-methylphenyl)amino]carbonyl}-2-{2-[(4-methylphenyl)amino]-2-oxoethyl}pyrimidin-4-yl)thio]acetyl}amino)-4,5,6,7-tetrahydro-1-benzo[b]thiophene-3-carboxylate

There total 3 articles about ethyl 2-({[(5-{[(4-methylphenyl)amino]carbonyl}-2-{2-[(4-methylphenyl)amino]-2-oxoethyl}pyrimidin-4-yl)thio]acetyl}amino)-4,5,6,7-tetrahydro-1-benzo[b]thiophene-3-carboxylate 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: 40.0%

2-chloroacetylamino-3-carbethoxy-4,5,6,7-tetrahydrobenzothiophene (60442-41-3) + N-(4-methylphenyl)-2-{2-[(4-methylphenyl)amino]-2-oxoethyl}-6-thioxo-1,6-dihydropyrimidine-5-carboxamide (1447585-56-9) → ethyl 2-({[(5-{[(4-methylphenyl)amino]carbonyl}-2-{2-[(4-methylphenyl)amino]-2-oxoethyl}pyrimidin-4-yl)thio]acetyl}amino)-4,5,6,7-tetrahydro-1-benzo[b]thiophene-3-carboxylate (1447585-64-9)

Guidance literature:

With potassium hydroxide; In ethanol; water; at 15 - 20 ℃; for 75h;

DOI:10.1007/s10593-013-1266-5

Reference yield:

2-cyano-N-(4-methylphenyl)acetamide (6876-54-6) → ethyl 2-({[(5-{[(4-methylphenyl)amino]carbonyl}-2-{2-[(4-methylphenyl)amino]-2-oxoethyl}pyrimidin-4-yl)thio]acetyl}amino)-4,5,6,7-tetrahydro-1-benzo[b]thiophene-3-carboxylate (1447585-64-9)

Guidance literature:

Multi-step reaction with 3 steps

1: pyridine; triethylamine; hydrogen sulfide

2: potassium hydroxide / ethanol / 54 h / 20 - 40 °C

3: potassium hydroxide / ethanol; water / 75 h / 15 - 20 °C

With pyridine; hydrogen sulfide; triethylamine; potassium hydroxide; In ethanol; water;

DOI:10.1007/s10593-013-1266-5

Reference yield:

3-amino-N-(4-methylphenyl)-3-thioxopropanamide (369609-88-1) → ethyl 2-({[(5-{[(4-methylphenyl)amino]carbonyl}-2-{2-[(4-methylphenyl)amino]-2-oxoethyl}pyrimidin-4-yl)thio]acetyl}amino)-4,5,6,7-tetrahydro-1-benzo[b]thiophene-3-carboxylate (1447585-64-9)

Guidance literature:

Multi-step reaction with 2 steps

1: potassium hydroxide / ethanol / 54 h / 20 - 40 °C

2: potassium hydroxide / ethanol; water / 75 h / 15 - 20 °C

With potassium hydroxide; In ethanol; water;

DOI:10.1007/s10593-013-1266-5

upstream raw materials:

2-chloroacetylamino-3-carbethoxy-4,5,6,7-tetrahydrobenzothiophene

N-(4-methylphenyl)-2-{2-[(4-methylphenyl)amino]-2-oxoethyl}-6-thioxo-1,6-dihydropyrimidine-5-carboxamide

2-cyano-N-(4-methylphenyl)acetamide

3-amino-N-(4-methylphenyl)-3-thioxopropanamide

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