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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1988807Generated: November 3, 2026

Pyridine → HCID 5275155, compound

https://huagongshe.com/reaction/1988807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-Bromo-n-(2-nitrophenyl)acetamideHCID 220787—
ReactantHCID 28887991HCID 28887991—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 5275155HCID 52751552.2%

Reaction Steps

A solution of 2,4-dihydro-4-(1-naphthalenyl)-3H-1,2,4-triazole-3-thione (129 mg, 0.50 mmol) in DMSO (2 mL) was added slowly to a solution of 2-bromo-N-(2-nitrophenyl)acetamide (113 mg, 0.50 mmol) and pyridine (121 μL, 1.49 mmol) in DMSO (1 mL) at room temperature. The mixture was stirred at room temperature for 18 h, then diluted with water and extracted with EtOAc (50 mL). The organic layer was washed with water (3×) and brine, dried (MgSO4), filtered and concentrated under reduced pressure. A mixture of Et2O and hexane (1:1) was added, the resulting suspension was filtered and the filtrate was concentrated under reduced pressure. The residue was purified by HPLC using a gradient of MeCN/H2O containing TFA (0.06%) (CombiPrep ODS-AQ 50×20 mm, 5μ, 120 Å). The pure fractions were combined and concentrated to give the title compound (4.5 mg, 2% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642277B2
Source datasetuspto-grants-2010_01
ORD IDord-3de7a3f32d4c4aca8d9eab505dd60f75
Source noteuspto-grants-2010_01