3-[4-(4-chlorophenyl)-2-(2-methyl-1H-imidazol-1-yl)-5-oxazolyl]propionic acid

Base Information

Chemical Name:3-[4-(4-chlorophenyl)-2-(2-methyl-1H-imidazol-1-yl)-5-oxazolyl]propionic acid
CAS No.:198064-11-8
Molecular Formula:C₁₆H₁₄ClN₃O₃
Molecular Weight:331.758
Hs Code.:

Synonyms:3-[4-(4-chlorophenyl)-2-(2-methyl-1H-imidazol-1-yl)-5-oxazolyl]propionic acid

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Chemical Property of 3-[4-(4-chlorophenyl)-2-(2-methyl-1H-imidazol-1-yl)-5-oxazolyl]propionic acid

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Technology Process of 3-[4-(4-chlorophenyl)-2-(2-methyl-1H-imidazol-1-yl)-5-oxazolyl]propionic acid

There total 9 articles about 3-[4-(4-chlorophenyl)-2-(2-methyl-1H-imidazol-1-yl)-5-oxazolyl]propionic acid 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: 84.0%

: 693-98-1
2-methylimidazole

: 198063-88-6
3-[2-chloro-4-(4-chlorophenyl)-5-oxazolyl]propionic acid

: 198064-11-8
3-[4-(4-chlorophenyl)-2-(2-methyl-1H-imidazol-1-yl)-5-oxazolyl]propionic acid

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 120 - 130 ℃; for 10h;
DOI:10.1248/cpb.51.565

Reference yield:

: 1501-26-4
methyl 4-(chlorocarbonyl)butyrate

: 198064-11-8
3-[4-(4-chlorophenyl)-2-(2-methyl-1H-imidazol-1-yl)-5-oxazolyl]propionic acid

Guidance literature:: Multi-step reaction with 8 steps

1: 91 percent / AlCl₃ / 2 h / 20 °C

2: 88 percent / Br₂ / CH₂Cl₂ / 20 °C

3: HCO₂Na / methanol / 12 h / Heating

4: 61.2 g / pyridine / tetrahydrofuran / 1 h / 20 °C

5: 79 percent / NH₄OAc; AcOH / 2 h / Heating

6: 73 percent / POCl₃; pyridine / 1.5 h / 125 °C

7: 96 percent / aq. NaOH / ethanol / 1 h / 20 °C

8: 84 percent / K₂CO₃ / dimethylformamide / 10 h / 120 - 130 °C

With pyridine; sodium hydroxide; aluminium trichloride; ammonium acetate; bromine; sodium formate; potassium carbonate; acetic acid; trichlorophosphate; In tetrahydrofuran; methanol; ethanol; dichloromethane; N,N-dimethyl-formamide; 1: Friedel-Crafts reaction;
DOI:10.1248/cpb.51.565

Reference yield:

: 71354-29-5
methyl 5-(4-chlorophenyl)-5-oxopentanoate

: 198064-11-8
3-[4-(4-chlorophenyl)-2-(2-methyl-1H-imidazol-1-yl)-5-oxazolyl]propionic acid

Guidance literature:: Multi-step reaction with 7 steps

1: 88 percent / Br₂ / CH₂Cl₂ / 20 °C

2: HCO₂Na / methanol / 12 h / Heating

3: 61.2 g / pyridine / tetrahydrofuran / 1 h / 20 °C

4: 79 percent / NH₄OAc; AcOH / 2 h / Heating

5: 73 percent / POCl₃; pyridine / 1.5 h / 125 °C

6: 96 percent / aq. NaOH / ethanol / 1 h / 20 °C

7: 84 percent / K₂CO₃ / dimethylformamide / 10 h / 120 - 130 °C

With pyridine; sodium hydroxide; ammonium acetate; bromine; sodium formate; potassium carbonate; acetic acid; trichlorophosphate; In tetrahydrofuran; methanol; ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1248/cpb.51.565