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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091572Generated: October 27, 2026

Ammonia → 4H-1,2,4-triazole-3-sulfonamide

https://huagongshe.com/reaction/1091572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHCID 178527437HCID 178527437—
SolventTetrahydrofuranHCID 8028—
Product4H-1,2,4-triazole-3-sulfonamideHCID 17851476254.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Liquid ammonia was added dropwise via a CO2/acetone condenser to a solution of 1H-1,2,4-triazole-3-sulfonyl chloride (500 mg, 2.98 mmol) in THF (5 mL) at −78° C. until the volume had approximately doubled (˜15 min). The reaction was stirred at −78° C. for 1 h and then allowed to slowly warm to rt. The reaction was concentrated to dryness and the residue was diluted with DCM. The slurry was filtered to remove the solids and the solution was concentrated to yield 1H-1,2,4-triazole-3-sulfonamide (240 mg, 1.620 mmol, 54.3% yield) as an off white solid. 1H NMR (300 MHz, CD3OD) δ ppm 8.60 (br s, 1H). LC-MS retention time 0.19 min; m/z 147 (MH−). LC data was recorded on a Shimadzu LC-10AS liquid chromatograph equipped with a Phenomenex-Luna 10 u C18 3.0×50 mm column using a SPD-10AV UV-Vis detector at a detector wave length of 220 nM. The elution conditions employed a flow rate of 5 ml/min, a gradient of 100% solvent A/0% solvent B to 0% solvent A/100% solvent B, a gradient time of 3 min, a hold time of 1 min, and an analysis time of 4 min where solvent A was 5% acetonitrile/95% H2O/10 mM ammonium acetate and solvent B was 5% H2O/95% acetonitrile/10 mM ammonium acetate. MS data was determined using a Micromass Platform for LC in electrospray mode.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129367B2
Source datasetuspto-grants-2012_03
ORD IDord-32547703fbe448aa88e5585b64e7104f
Source noteuspto-grants-2012_03