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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870859Generated: October 30, 2026

Lawesson's reagent → HCID 86701403, compound

https://huagongshe.com/reaction/870859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLawesson's reagentHCID 87949—
ReactantHCID 86701402HCID 86701402—
CatalystDiacetyloxymercuryHCID 16683746—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86701403HCID 8670140324%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969570B2
Source datasetuspto-grants-2015_03
ORD IDord-8f762226f67a47dcabb4c2324dbd17d9
Source noteuspto-grants-2015_03