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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509848Generated: October 30, 2026

Methanesulfonyl chloride → HCID 86658143, compound

https://huagongshe.com/reaction/1509848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 67424827HCID 67424827—
SolventDichloromethaneHCID 6344—
ProductHCID 86658143HCID 86658143100.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of (2,3-dihydro-4-oxa1-thia-6-aza-naphthalen-7-yl)-methanol (0.150 g, 0.8 mmol; prepared as described in WO 2004/058144) in DCM (4 mL), cooled to 0° C., were added TEA (0.228 mL, 1.6 mmol, 2 eq.) and MsCl (0.076 mL, 0.98 mmol, 1.2 eq.). The reaction was stirred at the same temperature. MsCl (0.013 mL, 0.16 mmol) was added after 30 min. A sat. NaHCO3 solution (25 mL) and DCM (20 mL) were added. The two layers were decanted and the org. layer was dried over Na2SO4, filtered and concentrated to dryness. The residue was purified by CC (DCM-MeOH 97-3) to afford the tittle compound as a yellowish oil (0.210 g, 98% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211890B2
Source datasetuspto-grants-2012_07
ORD IDord-84a53bf7b31743ed8dda115c32902e7e
Source noteuspto-grants-2012_07