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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915272Generated: November 1, 2026

(R)-propionic acid (acetyl-{3-[4-(1,1-dioxo-hexahydro-1lambda6-thiopyran-4-yl)-3-fluoro-phenyl]-2-oxo-oxazolidin-5-ylmethyl}-carbamoyloxy)-methyl ester → (S)-butyric acid 3-[4-(1,1-dioxo-hexahydro-1lambda6-thiopyran-4-yl)-3-fluoro-phenyl]-2-oxo-oxazolidin-5-ylmethylcarbamoyloxymethyl ester

https://huagongshe.com/reaction/915272

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-propionic acid (acetyl-{3-[4-(1,1-dioxo-hexahydro-1lambda6-thiopyran-4-yl)-3-fluoro-phenyl]-2-oxo-oxazolidin-5-ylmethyl}-carbamoyloxy)-methyl esterHCID 11386734—
Reactant((Chlorocarbonyl)oxy)methyl butyrateHCID 14800976—
SolventDichloromethaneHCID 6344—
Product(S)-butyric acid 3-[4-(1,1-dioxo-hexahydro-1lambda6-thiopyran-4-yl)-3-fluoro-phenyl]-2-oxo-oxazolidin-5-ylmethylcarbamoyloxymethyl esterHCID 5895856473%

Reaction Steps

Following general procedure C, (S)-5-aminomethyl-3-[4-(1,1-dioxo-hexahydro-1λ6-thiopyran-4-yl)-3-fluoro-phenyl]-oxazolidin-2-one (2) (492.7 mg, 1.44 mmol) in dichloromethane (13 mL) and butyroyloxymethyl carbonochloridate (7e) gave the titled product in 73% yield (512.1 mg, 1.05 mmol). 1H NMR (400 MHz, CDCl3): δ 7.48 (dd, 1H), 7.23 (t, 1H), 7.16 (dd, 1H), 5.73 (q, 2H), 5.29 (t, 1H), 4.80 (sept, 1H), 4.05 (t, 1H), 3.79 (dd, 1H), 3.67 (ddd, 1H), 3.56 (dt, 1H), 3.13-3.19 (m, 4H), 3.09 (dt, 1H), 2.35-2.47 (m, 2H), 2.31 (t, 2H), 2.14-2.22 (m, 2H), 1.63 (q, 2H), 0.93 (t, 3H). MS-APCI (m/z+): 487 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07265140B2
Source datasetuspto-grants-2007_09
ORD IDord-8218a7145ee348c6b65e054e9907cc87
Source noteuspto-grants-2007_09