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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449074Generated: October 26, 2026

Acetonitrile → 3-Methylureido-1-(gamma-sulfopropyl)-5-pyrazolone

https://huagongshe.com/reaction/1449074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantMethyl IsocyanateHCID 12228—
Reactant3-Hydrazinylpropane-1-sulfonic acidHCID 15566455—
ReactantEthylbeta-amino-beta-ethoxy acrylateHCID 86736826—
SolventAcetic AcidHCID 176—
SolventTriethylamineHCID 8471—
Product3-Methylureido-1-(gamma-sulfopropyl)-5-pyrazoloneHCID 20375087—

Reaction Steps

Into 30 ml of acetonitrile was dissolved 15.9 g of ethylβ-amino-β-ethoxy acrylate, and 6 g of methyl isocyanate was added thereto. The resulting mixture was allowed to stand at room temperature for two days. Into a mixed solution of 40 ml of glacial acetic acid and 20 ml of triethylamine there was dispersed 15.4 g of γ-hydrazinopropane sulfonic acid, and the above ester reaction solution was then added thereto and stirred while heating (95°-100° C.) on a water bath. In a short time, the solution became uniform and it was stirred as it was while heating (95°-100° C.) for 5 hours. The reaction solution was then concentrated under reduced pressure, and 50 ml of ethanol containing 35% by wt hydrogen chloride was then added to the resulting concentrated residue to thereby produce a uniform solution. This solution was allowed to stand in a refrigerator overnight and the crystals which precipitated were collected and recrystallized from methanol; thus, 14.8 g of crystals of the objective compound of a decomposition point of 186° C. was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04188489
Source datasetuspto-grants-1980_02
ORD IDord-5ae147f62de241d8b01590ddb16f5901
Source noteuspto-grants-1980_02