HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lawesson's reagent → HCID 86701403, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | HCID 86701402 | HCID 86701402 | — |
| Catalyst | Diacetyloxymercury | HCID 16683746 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86701403 | HCID 86701403 | 24% |
Reaction Steps
A solution of tert-butyl 4-(2-((2S,5R)-6-(benzyloxy)-7-oxo-1,6-diaza-bicyclo [3.2.1]octane-2-carbonyl)hydrazinecarbonothioyl)piperazine-1-carboxylate (0.66 g, 1.27 mmol) and Lawesson's reagent (0.36 g, 0.89 mmol) in THF (15 mL) was heated at 66° C. for 1 h, then cooled down to rt Hg(OAc)2 (0.4 g) was added and the mixture was stirred at rt overnight. The solution was then concentrated and the residue was purified by silica gel column chromatography (1:2 EtOAc/petroleum ether) to give tert-butyl 4-(5-((2S,5R)-6-(benzyloxy)-7-oxo-1,6-diaza-bicyclo[3.2.1]octan-2-yl)-1,3,4-thiadiazol-2-yl)piperazine-1-carboxylate (0.15 g, 24%) as a light yellow solid. ESI-MS (EI+, m/z): 501 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08969570B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-8f762226f67a47dcabb4c2324dbd17d9 |
| Source note | uspto-grants-2015_03 |