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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2412308Generated: November 2, 2026

Methane → HCID 13364715, compound

https://huagongshe.com/reaction/2412308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantHydrochloric AcidHCID 313—
ReactantThiazoleHCID 9256—
ReactantMethyl 2-[(4-methoxy-6-methyl-pyrimidin-2-yl)carbamoylsulfamoyl]benzoateHCID 13176578—
ReactantTrimethylaluminumHCID 16682925—
Reactant2H-1,2,3-Triazol-2-amineHCID 22600751—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 13364715HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04491467
Source datasetuspto-grants-1985_01
ORD IDord-83a66a3b7ad04acfacd3465558adb2f5
Source noteuspto-grants-1985_01