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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801490Generated: October 30, 2026

Ethyl Acetate → HCID 46929262, compound

https://huagongshe.com/reaction/1801490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium ethoxideHCID 2723922—
Reactant(E)-6-((dimethylamino)methylene)-6,11-dihydro-5H-dipyrido[2,3-b:4',3'-f]azepin-5-oneHCID 59506317—
ReactantHCID 178512446HCID 178512446—
SolventEthanolHCID 702—
ProductHCID 46929262HCID 4692926230.4%

Reaction Steps

A mixture of (E)-6-((dimethylamino)methylene)-6,11-dihydro-5H-dipyrido[2,3-b :4′,3′-f]azepin-5-one (0.303 g), 1-(3-chlorobenzyl)guanidinium chloride (0.500 g) and sodium ethoxide (21% solution in ethanol) (0.5 mL) in absolute ethanol (15 mL) was refluxed in for 3 hours. The reaction mixture was cooled to room temperature and poured into ethyl acetate (150 mL), washed with water (200 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure to yield a brown solid. The crude product was purified by flash chromatography (SiO2, gradient 100% ethyl acetate to 5% methanol in dichloromethane) to give the pure desired product, N-(3-chlorobenzyl)-9H-dipyrido[2,3-b:4′,3′-f]pyrimido[4,5-d]azepin-2-amine as a bright yellow solid (0.134 g). M.p.=195-196° C.; 1H NMR (DMSO-d6) 400 MHz δ 8.46-8.07 (m, 7H), 7.42-7.28 (m, 4H), 7.09 (brs, 1H), 4.58 (s, 2H); LCMS (M+H)=387.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349827B2
Source datasetuspto-grants-2013_01
ORD IDord-64eeb4d55ae84249a2c356f76c39d472
Source noteuspto-grants-2013_01