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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054210Generated: November 4, 2026

Hydrazine hydrate (1:1) → HCID 66966126, compound

https://huagongshe.com/reaction/1054210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 117925890HCID 117925890—
SolventEthanolHCID 702—
ProductHCID 66966126HCID 66966126135.4%

Reaction Conditions

Temperature75 °C

Reaction Steps

A mixture of methyl 3-picolinoylpicolinate 7, (240 mg, 0.99 mmol), hydrazine hydrate (63 μL, 1.3 mmol) and 12 mL of absolute ethanol was heated to 75° C. in a sealed tube for 1 h. After cooling, the solid was collected by vacuum filtration and dried under air suction. The mother liquor was concentrated to dryness under reduced pressure and purified by normal phase flash chromatography eluting with 0-10% methanol in dichloromethane over approximately 20 minutes. Like fractions were combined and concentrated under reduced pressure and combined with the solid collected by filtration to give 8-(pyridin-2-yl)pyrido[2,3-d]pyridazin-5(6H)-one 9 (150 mg, 0.67 mmol). 1H NMR (400 MHz, Methanol-d4) δ 9.07 (dd, J=4.5, 1.6 Hz, 1H), 8.98 (dd, J=8.4, 1.6 Hz, 1H), 8.72 (ddd, J=4.9, 1.7, 1.0 Hz, 1H), 8.00 (ddd, J=7.9, 7.3, 1.7 Hz, 1H), 7.99-7.92 (m, 1H), 7.97-7.84 (m, 1H), 7.53 (ddd, J=7.3, 4.9, 1.5 Hz, 1H). LCMS: (M+H)+, 225.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394299B2
Source datasetuspto-grants-2016_07
ORD IDord-f0c70623359e47cfa39c730c9c1d5cc0
Source noteuspto-grants-2016_07