反应 #2013

反应方程式

BOP

D-Homophenylalanine allyl ester

triethylamine

4-(benzyloxycarbonylamino)-4-methyl-pentanoic acid

→

(R)-α-[(4-Benzyloxycarbonylamino-4-methyl-1-oxopentyl)amino]benzenebutanoic acid allyl ester

溶剂

methylene chloride

methylene chloride

反应条件

后处理

1. 1
   workup.STIRRINGthis reaction mixture stirred at room temperature for 17 h
2. 2
   其他The reaction was quenched
3. 3
   workup.ADDITIONby adding brine
4. 4
   其他the products of the reaction isolated by extraction with methylene chloride (3×15 ml)
5. 5
   干燥dried with anhydrous magnesium sulfate powder
6. 6
   过滤filtered
7. 7
   其他evaporated under reduced pressure
8. 8
   其他A thick golden yellow gum was obtained which
9. 9
   其他was purified by column chromatography on silica gel
10. 10
    其他The product (182 mg; 48.9%) was isolated as a pale yellow gum

实验过程

D-Homophenylalanine allyl ester (175 mg; 0.80 mmol) (see Example 9, Step B), triethylamine (222 μl; 1.59 mmol) were dissolved in dry methylene chloride (2 ml) and 4-(benzyloxycarbonylamino)-4-methyl-pentanoic acid (211 mg; 0.80 mmol) added. The solution was stirred at room temperature and BOP (353 mg; 0.80 mmol) was added over 5 minutes, and this reaction mixture stirred at room temperature for 17 h. The reaction was quenched by adding brine and then the products of the reaction isolated by extraction with methylene chloride (3×15 ml). The methylene chloride layers were combined and dried with anhydrous magnesium sulfate powder, filtered and evaporated under reduced pressure. A thick golden yellow gum was obtained which was purified by column chromatography on silica gel using ethyl acetate and hexanes 1:2 v/v. The product (182 mg; 48.9%) was isolated as a pale yellow gum. FAB-MS:- calculated for C27H34 N2O5 466.3; found 467.7 (M+1).

来源