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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296028Generated: October 31, 2026

Cyclooctylamine → HCID 86739195, compound

https://huagongshe.com/reaction/2296028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclooctylamineHCID 2903—
ReactantN-{2-[({5-[(Dimethylamino)methyl]furan-2-yl}methyl)sulfanyl]ethyl}-1-(methylsulfanyl)-2-nitroethen-1-amineHCID 53427435—
SolventEthanolHCID 702—
ProductHCID 86739195HCID 8673919574.7%

Reaction Steps

A solution of 1-(methylthio)-1-[2-[[[5-(dimethylamino) methyl-2-furanyl]methyl]thio]ethylamino]2-nitroethene (1.05 g, 3.2 mmol) and cyclooctyl amine (1.2 g, 9.5 mmol) in ethanol (20 ml) was stirred at 20° C. for 21 days. The solvent was then removed in vacuo and the residue was chromatographed on a column of alumina (using chloroform as eluant) to give N-[2-[[[5-dimethylamino)-methyl-2-furanyl]methyl]thio]ethyl]-N'-cyclooctyl-2-nitro-1,1-ethenediamine (0.51 g, 39%) as an oil. [NMR τ (CDCl3) -0.30 br (s, 1H), 3.46 (s, 1H), 3.85 (s, 2H), 6.20 (s, 2H), 6.56 (s, 2H), 6.30-6.90 (m, 3H), 7.15-7.30 (m, 2H), 7.75 (s, 6H), 8.00-8.70 (m, 14H)]. [Found [M+H]+ 411.2391; C20H35N4O3S requires [M+H]+ 411.2429.]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04427685
Source datasetuspto-grants-1984_01
ORD IDord-25ab1ce45458490f81e64a685a53f442
Source noteuspto-grants-1984_01