反应 #1885046

反应方程式

(R)-3-hydroxy-1-phenylpyrrolidin-2-one

DIEA

triflic anhydride

(R)-3-(3,5-dichlorophenyl)pyrrolidine

→

(3R,3′S)-3-(3,5-dichlorophenyl)-1′-phenyl-1,3′-bipyrrolidin-2′-one

溶剂

DCM

water

DCM

反应条件

后处理

1. 1
   其他Synthesized
2. 2
   workup.STIRRINGthe reaction mixture was stirred at −20° C. for 1 hour
3. 3
   萃取extracted with EtOAc (3×)
4. 4
   洗涤The combined organic extracts were washed with water (2×), brine
5. 5
   干燥dried (Na2SO4)
6. 6
   其他evaporated to dryness
7. 7
   其他Purification by silica gel chromatography (30-60% EtOAc in hexane)

实验过程

Synthesized according to General Procedure 10. To a solution of (R)-3-hydroxy-1-phenylpyrrolidin-2-one (822 mg, 4.64 mmol) and DIEA (1.50 g, 2.02 mL, 11.59 mmol) in DCM (10 mL) at −20° C. was added triflic anhydride (1.57 g, 936 μL, 5.56 mmol) and the reaction mixture was stirred at this temperature for 20 min. A solution of (R)-3-(3,5-dichlorophenyl)pyrrolidine (835 mg, 3.86 mmol) in DCM (6 mL) was added and the reaction mixture was stirred at −20° C. for 1 hour. The reaction mixture was poured into water and extracted with EtOAc (3×). The combined organic extracts were washed with water (2×), brine, dried (Na2SO4) and evaporated to dryness. Purification by silica gel chromatography (30-60% EtOAc in hexane) gave (3R,3′S)-3-(3,5-dichlorophenyl)-1′-phenyl-1,3′-bipyrrolidin-2′-one as an oil that solidified upon standing (0.9 g, 62%). 1H-NMR (400 MHz, DMSO-d6) δ 7.67 (d, J=8.0 Hz, 2H), 7.42-7.36 (m, 5H), 7.15 (t, J=7.3 Hz, 1H), 3.77 (m, 2H), 3.52 (t, J=8.7 Hz, 1H), 3.05-2.98 (m, 4H), 2.88 (m, 1H), 2.31-2.23 (m, 2H), 2.06 (m, 1H) and 1.77-1.74 (m, 1H) ppm. LC/MS (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA), m/z: M+1 obs=375.5; tR=1.35 min.

来源