Ammonium Chloride → (4R)-1-[5-chloro-1-[(2,4-dimethoxyphenyl)sulfonyl]-3-(2-methoxy-5-methylphenyl)-2-oxo-2,3-dihydro-1H-pyrrolo[2,3-b]pyridin-3-yl]-4-hydroxy-N,N-dimethyl-L-prolinamide

참여 물질

반응 단계

To a solution of 500 mg of the compound obtained in Step 119-1 and 200 mg of Et3N in CHCl3 (5 ml) was added 207 mg of methane sulfonic acid anhydride under ice cooling. The solution was stirred at the same temperature for 20 minutes, then, 1.90 g of Et3N was added. Thereafter, a solution of (4R)-4-hydroxy-N,N-dimethyl-L-prolinamide trifluoroacetate (4.95 mmol) in CHCl3 (5 ml) was added dropwise at the same temperature. The solution was stirred at the same temperature for one hour, then, was gradually warmed and stirred for 30 minutes under room temperature conditions, then, was poured into a saturated aqueous solution of NH4Cl and extracted with CHCl3. The combined organic layer was washed with saturated brine, dried over Na2SO4, then, the drying agent was separated by filtration and the solvent was evaporated under reduced pressure. The obtained residue was separated and purified by column chromatography (first time: silicagel 60N; mobile phase: CHCl3/MeOH=10/0 to 9/1; v/v, first time: silicagel 60N; mobile phase: EtOAc/MeOH=10/0 to 9/1; v/v) to obtain respectively 7.6 mg (Isomer A: brown amorphous) and 18.9 mg (Isomer B: brown amorphous) of two species of diastereoisomers of the title compound.

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