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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 215689Generated: October 30, 2026

Hexyl isocyanate → HCID 59310298, compound

https://huagongshe.com/reaction/215689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexyl isocyanateHCID 75659—
ReactantMethyl 2-aminopyridine-3-carboxylateHCID 351633—
SolventPyridineHCID 1049—
ProductHCID 59310298HCID 5931029830.8%

Reaction Steps

17.46 g (137.3 mmol, 20 ml)n-hexyl isocyanate was added to a suspension of 5.31 g (34.9 mmol) 2-aminonicotinic acid methyl ester in 130 ml dry pyridine. The mixture was refluxed for 24 hours. The pyridine was removed under reduced pressure and the residue was treated with 160 ml ethanol. The mixture was refluxed for 10 minutes. The crude 3-hexyl-1H-pyrido[2,3-d]pyrimidine-2,4-dione crystallized from the medium and was purified by preparative column chromatography on straight phase silica (eluent:ethyl acetate:cyclohexane 1:2). 3-hexyl-1H-pyrido[2,3-d]pyrimidine-2,4-dione crystallized upon evaporation of the eluent. 2.66 g (310) of 3-hexyl-1H-pyrido[2,3-d]pyrimidine-2,4-dione was isolated (m.p. 166-168° C.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08192918B2
Source datasetuspto-grants-2012_06
ORD IDord-e2df6ccd7e454c438d3443803669cb68
Source noteuspto-grants-2012_06