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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482164Generated: November 2, 2026

Dichloromethane → HCID 178516268, compound

https://huagongshe.com/reaction/1482164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant2-AminopyridineHCID 10439—
Reactant2,3-DicyanohydroquinoneHCID 78467—
ReactantCalcium ChlorideHCID 5284359—
Solvent1-ButanolHCID 263—
SolventWaterHCID 962—
ProductHCID 178516268HCID 178516268—

Reaction Conditions

Temperature-40 °C

Reaction Steps

A solution of 1.0 g (6.24 mmol) 2,3-dicyanohydroquinone, 1.23 g (13.11 mmol) 2-aminopyridine and 0.14 g (1.3 mmol) CaCl2 in 20 ml 1-butanol was refluxed under N2. Despite the presents of fluorescent blue 2,3-dicyanohydroquinone starting material, as observed by TLC (CH2Cl2), the reaction was discontinued after 20 days. The reaction mixture was poured into 500 mL of H2O. The precipitate was collected by filtration and was washed with water until no blue fluorescents was observed from the filtrate. The precipitate was then dissolved in boiling CH2Cl2 and then cooled to −40° C. overnight. Precipitate was then collected by filtration and washed with MeOH. 0.485 g (24%), yellow needles. MS (Maldi-TOF): m/z=331.85. HRMS-FAB (m/z): [M+H]+ calcd for C18H14N5O2, 332.1142. found, 332.1136. 1H NMR (400 MHz, CDCl3), δ 13.3 (s, 1H), 8.57 (ddd, J=4.8, 2.0, 0.8 Hz, 2H), 7.75 (ddd, J=8.0, 7.6, 2.0 Hz, 2H), 7.35 (d, J=8.0 Hz, 2H), 7.11 (ddd, J=7.6, 4.8, 0.8 Hz, 2H), 7.00 (s, 2H). 13C NMR (100 MHz, CDCl3) δ 159.3, 154.9, 149.0, 147.9, 147.9, 138.1, 122.4, 121.4, 120.4, 116.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09412955B2
Source datasetuspto-grants-2016_08
ORD IDord-2933715962d14eb68f1c28b8c7762245
Source noteuspto-grants-2016_08