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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717572Generated: November 2, 2026

Methylhydrazine → 1-Methyl-5-(pyridin-2-yl)-1,4-dihydropyrimido[4,5-c]pyridazine

https://huagongshe.com/reaction/717572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylhydrazineHCID 6061—
ReactantSodium AcetateHCID 517045—
Reactant2-(4-Chloro-6-(pyridin-2-yl)pyrimidin-5-yl)acetaldehydeHCID 89815212—
SolventAcetonitrileHCID 6342—
Product1-Methyl-5-(pyridin-2-yl)-1,4-dihydropyrimido[4,5-c]pyridazineHCID 8981580660.5%

Reaction Steps

To a stirred solution of 2-(4-chloro-6-(pyridin-2-yl)pyrimidin-5-yl)acetaldehyde (600 mg) in dry MeCN (10 mL), methyl hydrazine (181 mg) and sodium acetate (422 mg) were added. The reaction mixture was stirred at room temperature for 3 hours and solvents were removed under reduced pressure. The resulting crude was purified by column chromatography using MeOH/CHCl3 (0.5:9.5) as eluent to afford 1-methyl-5-(pyridin-2-yl)-1,4-dihydropyrimido[4,5-c]pyridazine (350 mg) as white solid. 1H NMR (DMSO-d6): δ 3.41 (s, 3H), 3.93-3.94 (d, 2H), 6.92-6.94 (t, 1H), 7.47-7.51 (m, 1H), 7.94-7.99 (m, 1H), 8.00-8.10 (m, 1H), 8.67-8.69 (d, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193725B2
Source datasetuspto-grants-2015_11
ORD IDord-ac7f2ee0a0be415eb8e1c295575fa830
Source noteuspto-grants-2015_11