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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048572Generated: November 3, 2026

Methanesulfinic acid → HCID 58573831, compound

https://huagongshe.com/reaction/1048572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfinic acidHCID 87251—
ReactantSodiumHCID 5360545—
Reactant(3S,5S,6R,8S)-8-Allyl-6-(3-chloro-5-fluorophenyl)-5-(4-chlorophenyl)-3-ethyl-8-methyl-2,3,5,6,7,8-hexahydrooxazolo[3,2-a]pyridin-4-ium methanesulfonateHCID 86660748—
SolventAcetonitrileHCID 6342—
ProductHCID 58573831HCID 58573831—

Reaction Conditions

Temperature114 °C

Reaction Steps

To a solution of (3S,5S,6R,8S)-8-allyl-6-(3-chloro-5-fluorophenyl)-5-(4-chlorophenyl)-3-ethyl-8-methyl-2,3,5,6,7,8-hexahydrooxazolo[3,2-a]pyridin-4-ium methanesulfonate (Example 395, step A, 100 mg, 0.184 mmol) in MeCN (1.8 mL) was added methanesulfinic acid, sodium salt (56.5 mg, 0.553 mmol). The mixture was heated to 114° C. After heating for 24 hours, the mixture was cooled to room temperature and stirred for 2 days. The mixture was partitioned between EtOAc and aq. NH4Cl. The organic layer was washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated. The residue was purified by flash chromatography on silica gel (eluent: 20 to 60% EtOAc/hexanes, gradient elution) to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569341B2
Source datasetuspto-grants-2013_10
ORD IDord-1e131bfaa0c64632b9067d6bbdeba0bc
Source noteuspto-grants-2013_10