Реакция #2007

Уравнение реакции

benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate

D-Homophenylalanine benzyl ester

triethylamine

N-(t-butoxycarbonyl)-α-methylalanine

→

(R)-α-[(2-t-Butoxycarbonylamino-2-methyl-1-oxopropyl)amino]benzenebutanoic acid benzyl ester

Растворители

methylene chloride

methylene chloride

Условия реакции

Обработка

1. 1
   workup.STIRRINGThe reaction mixture was stirred at room temperature for 2.5 h
2. 2
   Другоеthen quenched
3. 3
   workup.ADDITIONby adding saturated brine (25 ml)
4. 4
   ЭкстракцияThe two phase system was extracted with methylene chloride (3×25 ml)
5. 5
   Сушкаthe combined methylene chloride extracts dried over magnesium sulfate powder
6. 6
   Фильтрацияfiltered
7. 7
   Другоеevaporated on a rotary evaporator under reduced pressure
8. 8
   Другоеto give a colorless oil that
9. 9
   Другоеon standing at room temperature
10. 10
    Другоеchromatographed on silica gel using an eluant
11. 11
    ДругоеThe product was isolated
12. 12
    Другоеafter evaporation of the volatiles as a white solid

Методика

D-Homophenylalanine benzyl ester (0.87 g; 3.23 mmol), triethylamine (900 ml) and N-(t-butoxycarbonyl)-α-methylalanine (656 mg; 3.23 mmol) were dissolved in dry methylene chloride (6.5 ml) and benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate (BOP-reagent) (1.43 g; 3.23 mmol) was added with stirring in small batches over 10 minutes. The reaction mixture was stirred at room temperature for 2.5 h then quenched by adding saturated brine (25 ml). The two phase system was extracted with methylene chloride (3×25 ml) and the combined methylene chloride extracts dried over magnesium sulfate powder, filtered and evaporated on a rotary evaporator under reduced pressure to give a colorless oil that solidified to an off white solid on standing at room temperature. This solid material was taken up in the minimum volume of methylene chloride and chromatographed on silica gel using an eluant composed of ethyl acetate and hexanes in the ratio 1:3 v/v. The product was isolated after evaporation of the volatiles as a white solid. The yield of the desired product was 1.30 g (88.5%). FAB-MS: -calculated for C26H34N2O5 454.2; found 455.5 (M+1).

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