تفاعل #78918

معادلة التفاعل

Mercaptoacetic acid

(L)-leucine methyl ester

triethylamine

p-chlorobenzaldehyde

→

4-Methyl-2-(S)-[2-(RS)-(4-chlorophenyl)-4-oxo-thiazolidin-3-yl]-pentanoic Acid Methyl Ester

المذيبات

dioxane

ethyl acetate

water

ظروف التفاعل

المعالجة

1. 1
   workup.ADDITION3 Å molecular sieves were added
2. 2
   درجة الحرارةThe mixture was heated at 80° C. for 4 hrs
3. 3
   workup.WAITthe heating was continued for an additional 12 hrs
4. 4
   درجة الحرارةThe reaction mixture was cooled to room temperature
5. 5
   ترشيحThe reaction mixture was filtered
6. 6
   أخرىto remove the molecular sieves
7. 7
   workup.ADDITIONThe organic layer was diluted with ethyl acetate (100 ml)
8. 8
   غسيلwashed twice with 60 ml of saturated solution of sodium carbonate, twice with aqueous 1N HCl and once with water
9. 9
   تجفيفThe organic layer was dried with MgSO4
10. 10
    أخرىevaporated
11. 11
    أخرىto give a residue that
12. 12
    أخرىwas carried out to the next step without further purification

الإجراء التجريبي

A suspension of (L)-leucine methyl ester (10 g, 55 mmol) and triethylamine (7.7 ml, 55 mmol) in 120 ml of dioxane was stirred at room temperature for 5 minutes. 3 Å molecular sieves were added followed by p-chlorobenzaldehyde (17 g, 121 mmol). The mixture was heated at 80° C. for 4 hrs. Mercaptoacetic acid (14.2 ml, 203.5 mmol) was added to the mixture and the heating was continued for an additional 12 hrs. The reaction mixture was cooled to room temperature, and diluted with ethyl acetate (40 ml) and water (30 ml). The reaction mixture was filtered to remove the molecular sieves. The organic layer was diluted with ethyl acetate (100 ml), washed twice with 60 ml of saturated solution of sodium carbonate, twice with aqueous 1N HCl and once with water. The organic layer was dried with MgSO4 and evaporated to give a residue that was carried out to the next step without further purification.

المصدر