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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383353Generated: October 31, 2026

Dichloromethane → HCID 54356446, compound

https://huagongshe.com/reaction/1383353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantMethyl morpholine oxideHCID 82029—
ReactantSodium BisulfateHCID 516919—
ReactantHCID 12444276HCID 12444276—
CatalystOsmium TetroxideHCID 30318—
Solventtert-ButanolHCID 6386—
SolventPropan-2-one--water (1/1)HCID 18366337—
ProductHCID 54356446HCID 5435644683%

Reaction Steps

To a stirred solution of the thiazepine prepared in Step 8 of Example 482 (243.7 mg) in 25% H2O/acetone (8 mL) is added 4-methylmorpholine N-oxide (201.5 mg) followed by a solution of osmium tetroxide in 2-methyl-2-propanol (2.5 wt %, 30 μL). The reaction mixture is stirred at room temperature for 18 h. The reaction mixture is treated with saturated sodium bisulfate (8 mL), then poured into CH2Cl2 (50 mL). The phases are separated. The aqueous phase is extracted with CH2Cl2 (2×25 mL). The combined organic phases are washed with brine (1×25 mL), dried (MgSO4), filtered and concentrated. The residue is purified on a Biotage 40 S column using 1% CH3OH in CH2Cl2 as the eluent to afford 216.1 mg (0.47 mmol, 83%) of the thiazepine S,S-dioxide as a white solid. mp 144-146° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06255304B1
Source datasetuspto-grants-2001_07
ORD IDord-71db70e11abf4018822782906e09054f
Source noteuspto-grants-2001_07