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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268745Generated: November 2, 2026

Methane → HCID 178432423, compound

https://huagongshe.com/reaction/2268745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantTriethylamineHCID 8471—
Reactant(1-Methylcyclohexyl)amine hydrochlorideHCID 3021577—
Reactant6-Chloro-3-fluoro-4H-thieno[3,2-e]-1,2,4-thiadiazine 1,1-dioxideHCID 10922691—
SolventEthanolHCID 702—
SolventSodium HydroxideHCID 14798—
ProductHCID 178432423HCID 1784324238%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 6-chloro-3-fluoro-4H-thieno[3,2-e]-1,2,4-thiadiazine 1,1-dioxide (0.5 g, 2.08 mmol), 1-methylcyclohexylamine hydrochloride (373 mg, 2.49 mmol) and triethylamine (0.58 ml, 4.16 mmol) in ethanol (3 ml) was stirred for 20 h at 50° C. and then for 22 h at 100° C. in a sealed flask. The cooled mixture was concentrated in vacuo and the residue was triturated with water followed by adjustment to pH <2 with 4M hydrochloric acid. The crude product was isolated by filtration and dissolved in 1 N sodium hydroxide followed by treatment with decolourising charcoal. After filtration, the solution was acidified to pH <2 with 4M hydrochloric acid and the precipitate was filtered off and purified by chromatography (dichloromethane/methanol (19:1)). Recrystallisation from ethanol afforded 55 mg (8%) of the pure title compound; mp 218-219° C.; 1H-NMR (DMSO-d6): δ1.18-1.54 (m, 11H), 1.97-2.12 (m, 2H), 6.55 (br s, 1H), 7.12 (s, 1H), 10.60 (br s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329367B1
Source datasetuspto-grants-2001_12
ORD IDord-722892babcab491890211558bc0a25b5
Source noteuspto-grants-2001_12