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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175187Generated: October 30, 2026

Water → HCID 58497414, compound

https://huagongshe.com/reaction/2175187

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-Nitropyridin-2-ylamineHCID 77887—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantEthyl 2-propylacrylateHCID 11844669—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 58497414HCID 5849741411.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of 2-amino-3-nitropyridine (390 mg, 2.80 mmol) in DMF (3 ml) was added ethyl 2-propylacrylate (500 mg, 3.52 mmol) followed by 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) (30 μl). The mixture was warmed to 80° C. and monitored by TLC (silica gel, 30% EtOAc/hexanes). After 48 hours, only starting material was detected by TLC. The reaction mixture was warmed to 100° C. for 4 days and cooled to room temperature. The reaction was poured into water and EtOAc. The layers were separated and the aqueous phase was extracted once more with EtOAc. The combined organics were dried (MgSO4), filtered and concentrated to give the crude product which was purified via silica gel flash column chromatography (Companion, 12 g silica gel, 15-50% EtOAc/hexanes). The product-containing fractions were combined and concentrated to give 90 mg (11%) of the desired compound which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062056B2
Source datasetuspto-grants-2015_06
ORD IDord-be1870efaac240b383319ae19885d4e5
Source noteuspto-grants-2015_06