(S)-4-(2-bromo-4-carbamoyl-phenyl)-6-methyl-2-thioxo-1-(3-trifluoromethyl-phenyl)-1,2,3,4-tetrahydro-pyrimidine-5-carboxylic acid methyl ester

Base Information

Chemical Name:(S)-4-(2-bromo-4-carbamoyl-phenyl)-6-methyl-2-thioxo-1-(3-trifluoromethyl-phenyl)-1,2,3,4-tetrahydro-pyrimidine-5-carboxylic acid methyl ester
CAS No.:1613621-88-7
Molecular Formula:C₂₁H₁₇BrF₃N₃O₃S
Molecular Weight:528.349
Hs Code.:

Synonyms:(S)-4-(2-bromo-4-carbamoyl-phenyl)-6-methyl-2-thioxo-1-(3-trifluoromethyl-phenyl)-1,2,3,4-tetrahydro-pyrimidine-5-carboxylic acid methyl ester

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Chemical Property of (S)-4-(2-bromo-4-carbamoyl-phenyl)-6-methyl-2-thioxo-1-(3-trifluoromethyl-phenyl)-1,2,3,4-tetrahydro-pyrimidine-5-carboxylic acid methyl ester

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Technology Process of (S)-4-(2-bromo-4-carbamoyl-phenyl)-6-methyl-2-thioxo-1-(3-trifluoromethyl-phenyl)-1,2,3,4-tetrahydro-pyrimidine-5-carboxylic acid methyl ester

There total 10 articles about (S)-4-(2-bromo-4-carbamoyl-phenyl)-6-methyl-2-thioxo-1-(3-trifluoromethyl-phenyl)-1,2,3,4-tetrahydro-pyrimidine-5-carboxylic acid methyl ester 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:

: 1613621-86-5
(S)-4-(2-Bromo-4-carboxy-phenyl)-6-methyl-2-thioxo-1-(3-trifluoromethyl-phenyl)-1,2,3,4-tetrahydro-pyrimidine-5-carboxylic acid methyl ester

: 1613621-88-7
(S)-4-(2-bromo-4-carbamoyl-phenyl)-6-methyl-2-thioxo-1-(3-trifluoromethyl-phenyl)-1,2,3,4-tetrahydro-pyrimidine-5-carboxylic acid methyl ester

Guidance literature:: (S)-4-(2-Bromo-4-carboxy-phenyl)-6-methyl-2-thioxo-1-(3-trifluoromethyl-phenyl)-1,2,3,4-tetrahydro-pyrimidine-5-carboxylic acid methyl ester; With 1,1'-carbonyldiimidazole; In tetrahydrofuran; at 20 ℃;

With ammonia; In tetrahydrofuran; water; at 10 - 20 ℃; for 2h;

Reference yield:

: 1403326-77-1
4-(dibromomethyl)-3-bromobenzoic acid

: 1613621-88-7
(S)-4-(2-bromo-4-carbamoyl-phenyl)-6-methyl-2-thioxo-1-(3-trifluoromethyl-phenyl)-1,2,3,4-tetrahydro-pyrimidine-5-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium carbonate / water; ethyl acetate / 4 h / 40 - 90 °C

2.1: polyphosphoric acid / tetrahydrofuran; diethyl ether / 20 h / -10 - 75 °C / Inert atmosphere

3.1: 1,4-dioxane / 3 h / 80 °C

4.1: hydrogenchloride / water; ethyl acetate

5.1: 1,1'-carbonyldiimidazole / tetrahydrofuran / 20 °C

5.2: 2 h / 10 - 20 °C

With hydrogenchloride; sodium carbonate; 1,1'-carbonyldiimidazole; In tetrahydrofuran; 1,4-dioxane; diethyl ether; water; ethyl acetate;

Reference yield:

: 1613621-85-4
4-(2-bromo-4-carboxyphenyl)-6-methyl-2-thioxo-1-(3-trifluoromethylphenyl)-1,2,3,4-tetrahydropyrimidine-5-carboxylic acid methyl ester

: 1613621-88-7
(S)-4-(2-bromo-4-carbamoyl-phenyl)-6-methyl-2-thioxo-1-(3-trifluoromethyl-phenyl)-1,2,3,4-tetrahydro-pyrimidine-5-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: 1,4-dioxane / 3 h / 80 °C

2.1: hydrogenchloride / water; ethyl acetate

3.1: 1,1'-carbonyldiimidazole / tetrahydrofuran / 20 °C

3.2: 2 h / 10 - 20 °C

With hydrogenchloride; 1,1'-carbonyldiimidazole; In tetrahydrofuran; 1,4-dioxane; water; ethyl acetate;