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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211170Generated: November 1, 2026

Methanesulfonic Acid → 5-[2-[(2,6-Dichloro-3-methylphenyl)amino]phenyl]-1,3,4-thiadiazol-2-amine

https://huagongshe.com/reaction/2211170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
Reactant2-[(2,6-Dichloro-3-methylphenyl) amino]-benzoic acid, 2-(aminothioxomethyl)hydrazideHCID 9864109—
SolventTolueneHCID 1140—
Product5-[2-[(2,6-Dichloro-3-methylphenyl)amino]phenyl]-1,3,4-thiadiazol-2-amineHCID 1495135859%

Reaction Steps

Methanesulfonic acid (280 μl, 4.31 mol) is added dropwise to a suspension of 2-[(2,6-dichloro-3-methylphenyl) amino]-benzoic acid, 2-(aminothioxomethyl)hydrazide (1.008 g, 2.73 mmol) in 30 ml of toluene. The mixture is heated at reflux for three hours under a nitrogen atmosphere and allowed to cool to room temperature overnight. The tan solid is filtered off and suspended in 100 ml of ethyl acetate. The suspension is then stirred vigorously with 40 ml of 10% aqueous ammonium hydroxide, and the layers are separated. The ethyl acetate layer is washed with water, and dried over magnesium sulfate. Filtration and concentration in vacuo gives a white solid. Drying at 60° C. in vacuo overnight provides 560.8 mg (59%) of product, mp 219°-226° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05462952
Source datasetuspto-grants-1995_10
ORD IDord-370bc1a58f0947b6a5efff668ee8450b
Source noteuspto-grants-1995_10