HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1099074Generated: October 30, 2026
Methanol → Methyl 4-(3-oxo-2,3-dihydro-1,2,4-triazin-6-yl)benzoate
https://huagongshe.com/reaction/1099074
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Semicarbazide hydrochloride | HCID 11236 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methyl 4-(diethoxyacetyl)benzoate | HCID 59216300 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 4-(3-oxo-2,3-dihydro-1,2,4-triazin-6-yl)benzoate | HCID 59216301 | — |
Reaction Steps
A mixture of methyl 4-(diethoxyacetyl)benzoate (15.4 g, 0.0578 mol), semicarbazide hydrochloride (7.1 g, 0.064 mol), N,N-diisopropylethylamine (12 mL, 0.069 mol) in 1,2-dichloroethane (150 mL), and methanol (2 mL) was heated at 95° C. for 4 h. To the mixture was added an additional 0.1 equivalents of semicarbazide hydrochloride. The mixture was stirred at 95° C. for 1 h. After cooling, the mixture was diluted with methylene chloride and washed with water and brine, dried over Na2SO4, filtered, and concentrated. The residue was refluxed with acetic acid (100 mL) and water (1.0 mL) overnight. The mixture was concentrated to yield quantitative crude material which was directly used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143251B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-831fa084038b49cda39bfbf91212f7e3 |
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| Source note | uspto-grants-2012_03 |
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