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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850709Generated: October 31, 2026

Water → HCID 18323161, compound

https://huagongshe.com/reaction/850709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-HydrazinopyridineHCID 78645—
ReactantHCID 18323185HCID 18323185—
ReactantPotassium tert-butoxideHCID 23665647—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18323161HCID 1832316160%

Reaction Conditions

Temperature5 °C

Reaction Steps

2 g (9 mmol) of methyl 2-isothiocyanato-2-phenylpropionate are dissolved in 30 ml of tetrahydrofuran. A solution containing 0.99 g of 2-hydrazinopyridine and 10 ml of tetrahydrofuran is added: the temperature of the mixture rises from 20 to 30° C. and a solid precipitates. The mixture is allowed to react for 0.5 hour at 30° C. and then is cooled to 5° C. A solution containing 1 g of potassium tert-butoxide and 10 ml of tetrahydrofuran is then added: the mixture becomes violet in color. The mixture is left to return to room temperature and is left to react for 2 hours. The mixture is poured into 150 ml of water. The mixture is neutralized with acetic acid. The product is extracted with 150 ml of ethyl acetate. The solution is washed with water, dried over magnesium sulfate and then treated with active charcoal. The solution is concentrated and the product is crystallized from 20 ml of diethyl ether. The above-mentioned product is filtered and is dried under vacuum. 1.6 g (yield: 60%) of 5-methyl-5-phenyl-3-(2-pyridylamino)-2-thiohydantoin is obtained as a pale-yellow solid melting at 80° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06018052
Source datasetuspto-grants-2000_01
ORD IDord-c4df7a82f9da46bc93897ae5dd69a741
Source noteuspto-grants-2000_01