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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | 3-Hydrazinylpropane-1-sulfonic acid | HCID 15566455 | — |
| Reactant | Ethylbeta-amino-beta-ethoxy acrylate | HCID 86736826 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 3-Methylureido-1-(gamma-sulfopropyl)-5-pyrazolone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04188489 |
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| Source dataset | uspto-grants-1980_02 |
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| ORD ID | ord-5ae147f62de241d8b01590ddb16f5901 |
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| Source note | uspto-grants-1980_02 |
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