HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662706Generated: October 30, 2026
Methanesulfonic anhydride → HCID 59867808, compound
https://huagongshe.com/reaction/1662706
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfonic anhydride | HCID 81560 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-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-one | HCID 67427767 | — |
| Reactant | (4R)-4-hydroxy-N,N-dimethyl-L-prolinamide trifluoroacetate | HCID 67429482 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 59867808 | HCID 59867808 | 1.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08030499B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-3fc2f732e38d458087fdd1d746c2f35f |
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| Source note | uspto-grants-2011_10 |
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