Hydrogen Bromide → HCID 22878404, compound

The HBr salt of the title product of Example 4 (1.00 g, 3.3 mmol) and 3,4-dichlorophenylacetic acid (1.07 g, 5.2 mmol, 1.5 eq) and DCC (1.43 g, 6.9 mmol, 2.0 eq) were reacted by addition of Et3N (2.4 mL, 5.0 eq) to give the title -compound (0.84 g, 92%) as a colorless crystalline solid. The reaction was-conducted as follows. To a stirred solution of the dichlorophenylacetic acid in CH2Cl2 (100 mL) was added a solution of the DCC in CH2Cl2 (100 mL) and the solution was stirred for 10 min at rt. To the precipitated complex was added the salt of the title compound of Example 4 followed by the Et3N and stirring was continued until TLC (solvent system A) indicated the reaction to -be complete. The precipitated DCU was removed by filtration and the filter cake was washed with Et20 (50 mL). The filtrate was diluted with enough Et20 to render the organic layer less dense than the aqueous layer, and the organic extract was then extracted with 10% aqueous -citric acid (200 mL) and discarded. The aqueous layer was washed with Et20 (2×200 mL) and the combined washings were discarded. The aqueous layer was basified by addition of excess concentrated aqueous NH3 solution and extracted with CH2Cl2 (2×200 mL). The combined organic layer was washed with water, dried (Na2SO4) and evaporated to give the desired product: mp 102.5-103.5° C. 2-propanol);

ORD record

ord-91bf45e7394a4f6285c7777200e26c40

Source dataset

uspto-grants-2001_10

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06310064B1