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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091571Generated: November 1, 2026

Ammonia → 2,4-Dimethylthiazole-5-sulfonamide

https://huagongshe.com/reaction/1091571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantDimethyl-1,3-thiazole-5-sulfonyl chlorideHCID 2776248—
SolventTetrahydrofuranHCID 8028—
Product2,4-Dimethylthiazole-5-sulfonamideHCID 1287318897%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Liquid ammonia was added dropwise via a CO2/acetone condenser to a solution of 2,4-dimethylthiazole-5-sulfonyl chloride (260 mg, 1.228 mmol) in THF (3 mL) at −78° C. until the volume had approximately doubled (˜10 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 CH2Cl2. The slurry was filtered to remove the solids and the solution was concentrated to yield 2,4-dimethylthiazole-5-sulfonamide (230 mg, 1.2 mmol, 97% yield) as a light yellow solid. LC-MS retention time 0.43 min; m/z 191 (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-c97b1b4cc3f54cae92d661eb8934a48c
Source noteuspto-grants-2012_03