HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243448Generated: October 31, 2026
2,4-Dihydro-5-methoxy-4-methyl-3H-1,2,4-triazol-3-one → Thiencarbazone-methyl
https://huagongshe.com/reaction/2243448
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Dihydro-5-methoxy-4-methyl-3H-1,2,4-triazol-3-one | HCID 10877145 | — |
| Reactant | 3-Thiophenecarboxylic acid, 4-(isocyanatosulfonyl)-5-methyl-, methyl ester | HCID 57957831 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | Thiencarbazone-methyl | HCID 11205153 | 93.2% |
Reaction Steps
12.9 g of 5-methoxy-4-methyl-2,4-dihydro-3H-1,2,4-triazol-3-one (3) (100 mmol) were initially charged in 200 ml of xylene and heated to 70° C. At this temperature, 119 g of a 22% solution of methyl 4-(isocyanatosulfonyl)-5-methylthiophene-3-carboxylate (2) (100 mmol) in dry xylene were metered in. The mixture was stirred at 70° C. for a further 5.8 h. Subsequently, workup was effected at room temperature by filtering the precipitated product. After washing with 50 ml of xylene and subsequently drying, 36.4 g of methyl 4-({[(3-methoxy-4-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl)carbonyl]amino}-sulfonyl)-5-methylthiophene-3-carboxylate (4) (91% of theory, content relative to standard: 97.5%) of melting point 201° C. were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07674917B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-d94f0249900f4f31b6326961710bc44e |
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| Source note | uspto-grants-2010_03 |
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