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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889106Generated: November 1, 2026

1,2,3-Thiadiazole-4-carboxylic acid, hydrazide → HCID 66599284, compound

https://huagongshe.com/reaction/1889106

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,3-Thiadiazole-4-carboxylic acid, hydrazideHCID 72720—
ReactantTriethyloxonium tetrafluoroborateHCID 2723982—
Reactant4-[(2,4-Dichloro-3-fluorophenyl)carbonyl]-2-piperazinoneHCID 66599361—
SolventDichloromethaneHCID 6344—
ProductHCID 66599284HCID 66599284—

Reaction Steps

Triethyloxonium tetrafluoroborate (363 mg, 1.908 mmol) was added to a suspension of 4-[(2,4-dichloro-3-fluorophenyl)carbonyl]-2-piperazinone (I37)(505 mg, 1.735 mmol) in dry dichloromethane (DCM) (4.2 ml). The reaction mixture was stirred at room temperature 45 mins—until everything was dissolved. 1,2,3-Thiadiazole-4-carbohydrazide (300 mg, 2.082 mmol, commercially available from e.g. Apollo) was added and the resulting mixture was stirred at room temperature for 3 h. DCM was evaporated and the residue was dissolved into 1-butanol (4.2 ml). The reaction mixture was stirred at reflux for 19 h. The mixture was washed with ethyl acetate and washed with water (2×25 mL) and brine (2×25 mL). The resulting organic layer was dried over MgSO4 and dried under reduced pressure. The crude product was purified by flash chromatography (DCM−10% MeOH in DCM). The residue was triturated with Et2O and then dried under vacuum at 50° C. for 2 days. The resulting solid was triturated with n-hexane and dried at 50° C. under vacuum 20 h to afford the desired product in 4.71 mg, as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501946B2
Source datasetuspto-grants-2013_08
ORD IDord-6838d906bbd0412bb1a8fdc4828ce91e
Source noteuspto-grants-2013_08