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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699227Generated: October 31, 2026

Hydrogen Sulfide → 2,4-dihydro-5-phenyl-2-[1-(9H-fluoren-9-ylmethoxycarbonyl)-4-piperidinyl]-3H-1,2,4-triazol-3-one

https://huagongshe.com/reaction/1699227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen SulfideHCID 402—
Reactant1,3-dihydro-5-methyl-4-phenyl-1-(4-piperidinyl)-2H-Imidazol-2-oneHCID 10825050—
Reactant(9H-fluoren-9-yl)methyl 4-hydrazinylpiperidine-1-carboxylateHCID 18321149—
SolventTetrahydrofuranHCID 8028—
Product2,4-dihydro-5-phenyl-2-[1-(9H-fluoren-9-ylmethoxycarbonyl)-4-piperidinyl]-3H-1,2,4-triazol-3-oneHCID 135627599—

Reaction Steps

The solutions of 5.56 g (0.0165 mol) of [1-(9H-fluoren-9-ylmethoxycarbonyl)-4-piperidinyl]-hydrazine in 60 ml of tetrahydrofuran and 3.7 g (0.0177 mol) of N-(ethoxycarbonyl)-benzothionamide in 30 ml of tetrahydrofuran were combined and refluxed for 1 hour, whereupon hydrogen sulphide was released. The solvent was distilled off in vacuo, the oily residue remaining was boiled with a little acetonitrile. The mixture was allowed to cool, then additionally cooled from outside with ice water and the resulting precipitate was suction filtered. 4.0 g (52% of theory) of colourless crystals were obtained, melting point 142° C. and Rf=0.38 (eluant 4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06344449B1
Source datasetuspto-grants-2002_02
ORD IDord-69fe663a75f640d0ac42d7a0b823b0be
Source noteuspto-grants-2002_02