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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306626Generated: November 2, 2026

Lawesson's reagent → HCID 10288183, compound

https://huagongshe.com/reaction/2306626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLawesson's reagentHCID 87949—
ReactantHCID 60066061HCID 60066061—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 10288183HCID 10288183112.9%

Reaction Steps

Lawesson's reagent (0.0715 g, 0.177 mmol) and {3-[3-fluoro-4-(5-oxo-5,6-dihydro-4H-[1,3,4]thiadiazin-2-yl)-phenyl]-2-oxo-oxazolidin-5(S)-ylmethyl}-carbamic acid tert-butyl ester (0.100 g, 0.236 mmol) in dioxane (5 ml) are heated at 65° C. for 6 hours. The reaction mixture is evaporated to dryness and the residue is purified by PTLC (10% MeOH/DCM) to give bright yellow solid (0.088 g, 85%); 1HNMR (300 MHz, DMSO-d6) δ 1.34 (s, 9H), 3.28 (t, J=5.5 Hz, 2H), 3.82 (dd, J=6.0, 9.1 Hz, 1H), 4.01 (s, 2H), 4.14 (t, J=9.3 Hz, 1H), 4.70-4.78 (m, 1H), 7.24 (t, J=5.8 Hz, 1H), 7.45 (dd, J=2.2, 8.8 Hz, 1H), 7.60 (dd, J=2.2, 14 Hz, 1H), 7.73 (t, J=8.8 Hz, 1H), 8.07 (t, J=6.0 Hz, 1H); mp 134-6; MS (m/z): [M+H]+=441.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06828317B2
Source datasetuspto-grants-2004_12
ORD IDord-b9c64964b6384c2097a1271e4e12ecff
Source noteuspto-grants-2004_12