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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662706Generated: October 30, 2026

Methanesulfonic anhydride → HCID 59867808, compound

https://huagongshe.com/reaction/1662706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic anhydrideHCID 81560—
ReactantSodium BicarbonateHCID 516892—
Reactant5-bromo-3-hydroxy-3-(2-methoxy-5-methylphenyl)-1-{[4-methoxy-2-(trifluoromethoxy)phenyl]sulfonyl}-1,3-dihydro-2H-pyrrolo[2,3-b]pyridin-2-oneHCID 67427767—
Reactant(4R)-4-hydroxy-N,N-dimethyl-L-prolinamide trifluoroacetateHCID 67429482—
SolventChloroformHCID 6212—
SolventTriethylamineHCID 8471—
ProductHCID 59867808HCID 598678081.7%

Reaction Steps

To a solution of 290 mg of the compound obtained in Step 120-5 and 97 mg of Et3N in CHCl3 (2 ml), on ice, was added 101 mg of methanesulfonic acid anhydride and the reaction mixture was stirred at room temperature for one hour. The solution was cooled again under ice cooling, 97 mg of Et3N and 261 mg of (4R)-4-hydroxy-N,N-dimethyl-L-prolinamide trifluoroacetate was added, and the reaction mixture was stirred at room temperature for two hours. A saturated aqueous solution of NaHCO3 was poured, and the solution was extracted with EtOAc. The 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 purified by thin layer chromatography (silicagel 60 F254; 1 mm thick; mobile phase: CHCl3/MeOH=9/1; v/v) to obtain 6 mg of the title compound (amorphous).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030499B2
Source datasetuspto-grants-2011_10
ORD IDord-3fc2f732e38d458087fdd1d746c2f35f
Source noteuspto-grants-2011_10