HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lawesson's reagent → HCID 10288183, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | HCID 60066061 | HCID 60066061 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 10288183 | HCID 10288183 | 112.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06828317B2 |
| Source dataset | uspto-grants-2004_12 |
| ORD ID | ord-b9c64964b6384c2097a1271e4e12ecff |
| Source note | uspto-grants-2004_12 |