HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186171Generated: November 3, 2026
Lawesson's reagent → HCID 76831279, compound
https://huagongshe.com/reaction/1186171
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 76831142 | HCID 76831142 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 76831279 | HCID 76831279 | — |
Reaction Steps
To a solution of (1SR,7RS)-1-[5-(benzhydrylidene-amino)-2-fluoro-phenyl]-5-oxa-2-aza-bicyclo[5.1.0]octan-3-one (intermediate B11A) (460 mg, 1.15 mmol) in dioxane (3 ml) at 23° C. was added 2,4-bis-(4-methoxy-phenyl)-[1,3,2,4]dithiadiphosphetane 2,4-disulfide (Lawesson's reagent) (292 mg, 0.72 mmol) and the mixture was stirred at 80° C. for 2 h. The green solution was poured on sat. NaHCO3 solution, extracted with ethyl acetate, washed the organic layer with brine and dried over sodium sulfate. Removal of the solvent in vacuum left the title compound as a green oil (600 mg, ca. 80% pure, 100%), which was used in the next step without further purification. MS (ISP): m/z=417.3 [(M+H)+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08673894B2 |
|---|
| Source dataset | uspto-grants-2014_03 |
|---|
| ORD ID | ord-8fae6fdb41674d34aae730c4c0eff121 |
|---|
| Source note | uspto-grants-2014_03 |
|---|