methyl 6-chloro-4-(3,4-difluorophenyl)-4-methyl-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate

Base Information

• Chemical Name: methyl 6-chloro-4-(3,4-difluorophenyl)-4-methyl-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate
• CAS No.: 1446680-73-4
• Molecular Formula: C₁₆H₁₂ClF₂N₃O₂S
• Molecular Weight: 383.806
• Mol file: 1446680-73-4.mol

Synonyms:methyl 6-chloro-4-(3,4-difluorophenyl)-4-methyl-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate

Chemical Property of methyl 6-chloro-4-(3,4-difluorophenyl)-4-methyl-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of methyl 6-chloro-4-(3,4-difluorophenyl)-4-methyl-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate

There total 3 articles about methyl 6-chloro-4-(3,4-difluorophenyl)-4-methyl-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-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:

methyl 4-(3,4-difluorophenyl)-4-methyl-6-oxo-2-(thiazol-2-yl)-1,4,5,6-tetrahydropyrimidine-5-carboxylate (1446680-72-3) → methyl 6-chloro-4-(3,4-difluorophenyl)-4-methyl-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate (1446680-73-4)

Guidance literature:

With trichlorophosphate; at 120 ℃; for 1.25h; Sealed tube;

Reference yield:

4-ethynyl-1,2-difluorobenzene (143874-13-9) → methyl 6-chloro-4-(3,4-difluorophenyl)-4-methyl-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate (1446680-73-4)

Guidance literature:

Multi-step reaction with 3 steps

1: indium(III) chloride / 18 h / 130 °C / Sealed tube

2: N,N-dimethyl-formamide / 6 h / 60 °C

3: trichlorophosphate / 1.25 h / 120 °C / Sealed tube

With indium(III) chloride; trichlorophosphate; In N,N-dimethyl-formamide;

Reference yield:

C13H12F2O4 (1446679-57-7) → methyl 6-chloro-4-(3,4-difluorophenyl)-4-methyl-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate (1446680-73-4)

Guidance literature:

Multi-step reaction with 2 steps

1: N,N-dimethyl-formamide / 6 h / 60 °C

2: trichlorophosphate / 1.25 h / 120 °C / Sealed tube

With trichlorophosphate; In N,N-dimethyl-formamide;

upstream raw materials:

4-ethynyl-1,2-difluorobenzene

C₁₃H₁₂F₂O₄

methyl 4-(3,4-difluorophenyl)-4-methyl-6-oxo-2-(thiazol-2-yl)-1,4,5,6-tetrahydropyrimidine-5-carboxylate

Downstream raw materials:

(R)-4-(3,4-difluoro-phenyl)-4,6-dimethyl-2-thiazol-2-yl-1,4-dihydro-pyrimidine-5-carboxylic acid methyl ester

(S)-4-(3,4-difluoro-phenyl)-4,6-dimethyl-2-thiazol-2-yl-1,4-dihydro-pyrimidine-5-carboxylic acid methyl ester

4-(3,4-difluoro-phenyl)-4,6-dimethyl-2-thiazol-2-yl-1,4-dihydro-pyrimidine-5-carboxylic acid methyl ester