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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953149Generated: November 3, 2026

Pyridine → HCID 136395932, compound

https://huagongshe.com/reaction/1953149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 9838563HCID 9838563—
SolventEthanolHCID 702—
ProductHCID 136395932HCID 13639593289.2%

Reaction Steps

To a solution of 0.5 g (1.79 mmol) of 3-(oxophenylmethyl)-1,2,4-thiadiazolo[4,5-a]benzimidazole in 7 mL of ethanol was added 0.5 mL (6.46 mmol) of pyridine and 0.5 g (7.20 mmol) of hydroxylamine hydrochloride. The mixture was refluxed for overnight. The precipitate was collected by filtration, and washed with methanol and dichloromethane to give the crude product, which was recrystallized from methanol to yield 0.47 g (89%) of the title compound as white crystals. mp 247° C.; 1H NMR (DMSO-d6)δ 11.89 (s, 1H), 7.81 (d, 1H), 7.73 (dd, 2H), 7.45-7.53 (m, 5H), 7.32 (t, 1H) ppm; 13C NMR (CDCl3)δ 168.25, 155.24, 150.52, 147.95, 136.94, 135.67, 134.30(2C), 133.03, 131.52(2C), 130.35, 127.26, 124.28, 116.91 ppm; IR (KBr)δ 2731, 1549, 1475, 1450, 1251, 1194, 983, 753, 736 cm-1HRMS calcd for C15H10N4OS 294.0575, found 294.0583

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06114537
Source datasetuspto-grants-2000_09
ORD IDord-cb9722aa76df4937957c0d366c00ea45
Source noteuspto-grants-2000_09