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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 909475Generated: November 1, 2026

Sodium Bicarbonate → HCID 58065503, compound

https://huagongshe.com/reaction/909475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant(Bis(2-methoxyethyl)amino)sulfur trifluorideHCID 2734690—
ReactantHCID 58065449HCID 58065449—
SolventDichloromethaneHCID 6344—
ProductHCID 58065503HCID 5806550361%

Reaction Steps

[2-(5-{3-[(1S)-2-Methoxy-1-methylethoxy]-5-[4-(methylsulfonyl)phenoxy]phenyl}-1H-pyrrol-2-yl)-4,5-dihydro-1,3-oxazol-5-yl]methanol (100 mg, 0.20 mmol) synthesized in Example 29 was dissolved in dichloromethane (5 mL), and bis(2-methoxyethyl)aminosulfur trifluoride (81 μL, 0.44 mmol) was added at 0° C. After stirring at room temperature for 6 hours, a saturated aqueous sodium hydrogencarbonate solution was added, and extraction was carried out with dichloromethane (60 mL). The organic layer was washed with saturated brine, and subsequently dried over sodium sulfate. The solvent was distilled off under reduced pressure, and the resulting residue was purified using silica gel column chromatography (elution solvent: ethyl acetate/hexane=80%-100%) to afford the desired product (61 mg, yield 61%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017610B2
Source datasetuspto-grants-2011_09
ORD IDord-88aaf6a42c2b4b0e9c3d6b63b1c2201f
Source noteuspto-grants-2011_09