Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Thiazole | HCID 9256 | — |
| Reactant | Methyl 2-[(4-methoxy-6-methyl-pyrimidin-2-yl)carbamoylsulfamoyl]benzoate | HCID 13176578 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | 2H-1,2,3-Triazol-2-amine | HCID 22600751 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 13364715 | HCID 13364715 | — |
Reaction Steps
To a solution of 2-aminotriazole (2.1 g) in 100 ml of methylene chloride was added 10 ml of a 2M solution in toluene of trimethylaluminum (1.44 g of Al(CH3)3) by syringe. Evolution of methane gas was seen and the solution became homogeneous. To this mixture was added 4.0 g of N-[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]-2-methoxycarbonylbenzenesulfonamide and the homogeneous solution was heated at reflux for 18 hours. The reaction mixture was then heated with aqueous hydrochloric acid and the precipitated product isolated by filtration, 1.42 g, m.p. 185°-187° C. IR: 1690 cm-1 and 1700 cm-1 unresolved double carbonyl, NMR: in TFA 2.7 ppm s, CH3 pyrimidine, 4.2 ppm s, OCH3 on pyrimidine, 6.7 ppm s, proton in 5-position on pyrimidine, 7.8-8.0 ppm and 8.4-8.5 ppm M, aromatic, 7.6, 7.7 ppm D, thiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04555261 |
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| Source dataset | uspto-grants-1985_11 |
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| ORD ID | ord-55ccb0bf8949465fbeb2da71e6558fbb |
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| Source note | uspto-grants-1985_11 |
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