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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915291Generated: October 31, 2026

Water → HCID 11204102, compound

https://huagongshe.com/reaction/915291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium IodideHCID 5238—
ReactantHCID 58958555HCID 58958555—
ReactantHCID 86601882HCID 86601882—
SolventAcetonitrileHCID 6342—
ProductHCID 11204102HCID 1120410275%

Reaction Steps

(R)-acetyl-{3-[4-(1,1-dioxo-hexahydro-1λ6-thiopyran-4-yl)-3-fluoro-phenyl]-2-oxo-oxazolidin-5-ylmethyl}-carbamic acid chloromethyl ester (10) (0.40 g, 0.84 mmol), cesium 2(S)-phenyl-propionate (0.37 g, 1.31 mmol) and sodium iodide (0.13 g, 0.86 mmol) in acetonitrile (25 mL) are heated to reflux overnight. After cooling to RT, water is added and the reaction mixture is extracted with EtOAc and then with dichloromethane. The organic phases are washed separately with brine and then the organic layers are combined, dried over MgSO4, filtered, and conc in vacuo. The isolated residue is subjected to silica gel flash chromatography, eluting with MeOH/CH2Cl2 gradient (0-5% MeOH over 1 hour and 20 minutes) to afford the title compound. Isolated yield: 75%. 1H NMR (400 MHz, DMSO-d6): δ 7.43-7.39 (m, 1H), 7.33 (t, 1H), 7.27-7.15 (m, 6H), 5.78-5.72 (m, 2H), 4.63-4.57 (m, 1H0, 4.02-3.95 (m, 2H), 3.84 (q, 1H), 3.76-3.69 (m, 2H), 3.36-3.26 (m, partially obscured by water, 2H), 3.18-3.12 (m, 1H), 3.07-3.04 (m, 2H), 2.30 (d, 3H), 2.11 (q, 2H), 2.01-1.97 (m, 2H), 1.35 (d, 3H); MS-APCI (m/z+): 341, 385, 517, 591.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07265140B2
Source datasetuspto-grants-2007_09
ORD IDord-10b17f39d27b4d3bbd88f3cb2021413e
Source noteuspto-grants-2007_09